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positioning. . . . . . . . . . . . . . . . . . . . . . . . . . . . 4
Step 2: Discectomy and endplate preparation . . . . . . 5
Step 3: Disc elevation . . . . . . . . . . . . . . . . . . . . . . . . . 6
Step 4: Determining interbody size . . . . . . . . . . . . . . 7
Step 5: Interbody selection . . . . . . . . . . . . . . . . . . . . . 8
Step 6: Interbody insertion. . . . . . . . . . . . . . . . . . . . 10
Step 7: Drill guides . . . . . . . . . . . . . . . . . . . . . . . . . . 14
Step 8: Create pilot hole and drill . . . . . . . . . . . . . . . .
vertebral body. . . . . . . . . . . . . . . . . . . . . . . . 16
Step 9: Screw preparation and insertion. . . . . . . . . 17
Step 10: Final locking . . . . . . . . . . . . . . . . . . . . . . . . 18
Step 11: Implant removal . . . . . . . . . . . . . . . . . . . . . 20
Product catalog
Trials . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 22
Instruments. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 24
Implants. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 31
This publication sets forth detailed recommended procedures for using the Chesapeake Anterior-Lumbar Stabilization
System. It offers guidance that you should heed, but, as with any such technical guide, each surgeon must consider the
particular needs of each patient and make appropriate adjustments when and as required.
2 Surgical technique
Surgical technique
Cranial
Caudal
4 Surgical technique
Step 2
#4 Forward Angled Curette 4mm Anterior Pituitary 8mm Double Action Curette Connector Shaft
Rongeur 45° Rongeur
Disc elevation
A Disc Spreader may be inserted as a temporary
spacer while additional preparation is performed on
the contralateral side. Modular Disc Spreaders, which
connect to a Fixed T-Handle, are included in the set.
6 Surgical technique
Step 4
Interbody selection
An appropriately sized interbody is chosen at the Note: 21mm height is only available in
discretion of the surgeon. The interbody should hyperlordotic implant options.
be securely seated with a tight fit between the
endplates when the segment is fully distracted is
rcommended. Implants are sized at 24 x 30, 28 x 36,
and 30 x 40mm footprints. Each of these footprints
is available in 5°, 10°, 15°, 20°, 25°, and 30° lordotic
angles in heights ranging from 11 - 21mm in 2mm
increments.
24mm
28mm
30mm
36mm
30mm
40mm
8 Surgical technique
Each footprint includes a color-coded SMARTLock
insert to easily indentify the degrees of lordosis. The
height of the interbody is measured from tip-of-
tooth to tip-of-tooth.
Interbody insertion
Insertion option 1: Anterior Insertion Ramp Steps:
1. Hold the instrument vertically to allow the
The Anterior Insertion Ramp utilizes a controlled distraction ramps to open.
threaded mechanism which is designed to provide 2. Insert the inner shaft through the proximal end
parallel distraction, resulting in a zero-impact load of the Inserter and rotate clockwise 1-2 turns to
on the implant. To help ensure proper use of the engage the threads.
Anterior Insertion Ramp, complete the following 3. Place the Chesapeake Modular Tip over the Inner
Shaft.
10 Surgical technique
4. Turn the gold thumbwheel clockwise and 8. Rotate the Anterior Insertion Ramp 180° to close
finger tighten until the threads disappear and the distraction ramps.
components mate flush. 9. Place the distal end of the distraction ramps into
5. Attach the implant to the Chesapeake Modular the disc space until the Vertebral Body Stops
Tip. make contact with the anterior surface of the
6. Final tighten the implant by turning the knob vertebrae.
of the inner shaft on the proximal end of the 10. Turn the T-Handle clockwise to advance the
Inserter. implant into the disc space.
7. Adjust the countersink depth on the Anterior
Insertion Ramp from 0 - 6mm by rotating
the silver knurled thumbwheel behind the
countersink depth bar on the modular tip.
11. When the Countersink Depth Bar makes contact 12. Disengage the implant by turning the Inner Shaft
with the vertebral bodies, the Anterior Insertion knob on the proximal end of the Inserter counter-
Ramp is designed to begin to remove itself from clockwise.
the disc space, while maintaining the position of 13. Completely remove the Inner Shaft for cleaning
the implant according to the pre-set countersink once insertion is complete.
depth. Continue to thread the inner shaft until the
distraction ramp is fully removed from the disc
space. Fluoroscopy can be used to confirm the
final position of the implant before removing the
insertion ramp.
12 Surgical technique
Insertion option 2: Chesapeake Implant Inserter
1. Insert the Inner Shaft through the proximal end 4. After the implant is properly seated in the
of the Inserter and rotate clockwise 1–2 turns to disc space, turn the Inner Shaft knob at the
engage the threads. proximal end of the Inserter counter-clockwise to
2. Load the interbody onto the Chesapeake Implant disengage the implant.
Inserter.
3. Turn the inner shaft thumbwheel on the proximal Care must be taken to protect the vascular elements
end of the Implant Inserter in a clockwise before removing the Chesapeake Implant Inserter
direction to secure the implant. The Large Mallet from the surgical site. If needed, the Removal Tool
may be used to aid in implant placement. X-ray may be used to adjust the implant anteriorly.
or fluoroscopy may be used live or periodically to
verify placement.
Drill guides
Two Drill Guides are available for use: A Single
Barrel Drill Guide and a Expandable Drill Guide.
The Single Barrel Drill Guide is used to awl and drill
at a fixed trajectory of 35°. The Expandable Drill
Guide is used to awl, tap, drill, and insert screws at
a fixed trajectory of 40°. Expandable Drill Guides are
available in sequential heights from 11 - 19mm in
2mm increments.
14 Surgical technique
The Three Barrel Drill Guides correspond to each
interbody height. Load the Three Barrel Drill Guide
onto the distal end of the Drill Guide Inserter by
pulling back on the outer shaft of the Drill Guide
Inserter to secure. Insert the instrument into the
interbody making sure to match up the markings for
correct screw orientation. Turn the green silicone
handle clockwise to secure the Three Barrel Drill
Guide to the interbody.
20mm Spring Loaded Chesapeake Ratcheting 20mm Awl 20mm Universal Awl
Punch Awl Hudson Handle
20mm Drill 20mm Universal Drill 20mm Tap 20mm Universal Tap
16 Surgical technique
Step 9
Final locking
Final screw locking should only be performed When the screw head engages on the locking lip of
once the screw positions have been verified via the SMARTLock insert, the insert will lag down to
intra-operative radiographs. Once the screws are the bone and the SMARTLock technology is designed
tightened, they are designed to become locked to the to engage. Due to a difference in material hardness
SMARTLock insert. and design, the screw head begins to deform the
SMARTLock insert through a reshaping process and
Use the Size 20 Non-Tapered Driver attached to the thus forms an autogenic lock.
Gray Torque Limiting Handle to final tighten the
screws to 20 in-lbs.
18 Surgical technique
The Torque Limiting Handle emits an audible “click” Note: If hyperlordotic interbodies (20°, 25°, and 30°)
at 20 in-lbs to signify the screw has formed an were implanted, supplemental fixation (posterior)
autogenic lock with the SMARTLock insert. Use of is required. See the Mesa Spinal System, Everest
the Torque Limiting Handle further helps ensure Spinal System or Serengeti Minimally Invasive
that the screw is not over tightened. No additional Retractor System Surgical Techniques for additional
locking step is required. instruction.
Implant removal
If screw removal is required, each screw may be
unlocked using the Ratcheting Hudson Handle and
Size 20 Tapered Driver. If interbody removal is
required, use the Chesapeake Implant Inserter or
Removal Tool.
Chesapeake Ratcheting
Hudson Handle
20 Surgical technique
Product catalog
Description Heights
24 x 30mm Trial 9 - 21mm Unique catalog numbers exist for each Trial in each
footprint, height, and degree of lordosis. Please
28 x 36mm Trial 9 - 21mm
contact your local sales consultant with any
questions you may have about the Chesapeake
Anterior-Lumbar Stabilization System.
Note: 9mm Trials are for use with the Aleutian Anterior-Lumbar Interbody System.
21mm Trials are for use with the Chesapeake Anterior-Lumbar Interbody System.
22 Product catalog
Trials
Description Heights
Unique catalog numbers exist for each Trial in each
30 x 40mm Trial 11 – 21mm
footprint, height, and degree of lordosis. Please
contact your local sales consultant with any
questions you may have about the Chesapeake
Anterior-Lumbar Stabilization System.
#2 Straight Curette
#4 Straight Curette
#2 Serrated Curette
#4 Serrated Curette
Curette Handle
24 Product catalog
Instruments
602-90225 Fixed T-Handle with Hudson 702-90099 13” 4mm Anterior Pituitary Rongeur with Teeth
702-90068 Large Cobb 702-90100 13” 6mm Anterior Pituitary Rongeur with Teeth
702-90067 Small Cobb 702-90101 8mm Double Action Rongeur
702-90158 15mm Chisel 702-90066 Large Scalpel Blade Holder
702-90159 17mm Chisel 702-90182 Small Scalpel Blade Holder
702-90208 Pusher
702-90098 13” 4mm Anterior Pituitary Rongeur 45°
702-90157 13” 6mm Anterior Pituitary Rongeur 45°
Large Cobb
Small Cobb
15mm Chisel
17mm Chisel
Pusher
Catalog # Description
Angled Rasp
Convex Rasp
Trial Inserter
Large Mallet
Slap Hammer
26 Product catalog
Instruments
Catalog # Description
20mm Tap
20mm Awl
20mm Drill
Catalog # Description
28 Product catalog
Instruments
Catalog # Description
Catalog # Description
Removal Tool
30 Product catalog
Implants
Description Heights
Screws
Description Lengths Unique catalog numbers exist for each screw length
Ø5.5mm 20, 25, and 30mm
for each degree of lordosis. Please contact your local
sales consultant with any questions you may have
about the Chesapeake Anterior-Lumbar Stabilization
System.
Ø5.5mm Screws
Lengths (mm): 20, 25, 30
IFU Reference
Number:
34 Notes
Chesapeake | Anterior-Lumbar Stabilization System 35
Spine division Manufactured by:
A surgeon must always rely on his or her own professional clinical judgment when deciding whether to use a particular product when K2M, Inc.
treating a particular patient. Stryker does not dispense medical advice and recommends that surgeons be trained in the use of any
particular product before using it in surgery. 600 Hope Parkway SE
Leesburg, VA 20175
The information presented is intended to demonstrate the breadth of Stryker product offerings. A surgeon must always refer to the package
insert, product label and/or instructions for use before using any Stryker product. The products depicted are CE marked according to t: 571 919 2000
either the Medical Device Directive 93/42/EEC or Regulation (EU) 2017/745. Products may not be available in all markets because product
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