Cleared Special

K262061 - Tritanium® C Anterior Cervical Cage

Also marketed or referenced as:
Tritanium® PL Cage Tritanium® TL Curved Posterior Lumbar Cage Aero® -C Cervical Cage System AVS® Anchor-C Cervical Cage System AVS® TL PEEK Spacer AVS® PL PEEK Spacers AVS® Navigator PEEK Spacer AVS® AS PEEK Spacer Monterey™ AL Interbody System Aleutian IBF System Cascadia Interbody System Chesapeake Stabilization System Sahara Stabilization System SANTORINI™ Corpectomy Cage System MOJAVE Interbody System VLIFT VERTEBRAL BODY REPLACEM

K262061 is an FDA 510(k) clearance for Tritanium C Anterior Cervical Cage, manufactured by Stryker Spine. The device is a Class 2 Orthopedic device with product code ODP cleared through the Special 510(k) pathway after a 29-day FDA review.

K262061 · Stryker Spine · Orthopedic device
Download Printable Device Report (PDF)
Optimized for regulatory review, auditing and printing
Jul 2026
Decision
29d
Days
Class 2
Risk

K262061 is an FDA 510(k) clearance for the Tritanium® C Anterior Cervical Cage. Classified as Intervertebral Fusion Device With Bone Graft, Cervical (product code ODP), Class II - Special Controls.

Submitted by Stryker Spine (Allendale, US). The FDA issued a Cleared decision on July 17, 2026 after a review of 29 days - a notably fast clearance cycle.

This device falls under the Orthopedic FDA review panel, regulated under 21 CFR 888.3080 - the FDA orthopedic device regulatory framework. As a Special 510(k), this submission covers a manufacturer modification to an existing cleared device rather than a new device introduction.

Device pattern: Iterative device modification. Low regulatory complexity profile. This Special 510(k) clearance confirms that the manufacturer's modifications remained within the established regulatory envelope of the original cleared device.

View all Stryker Spine devices

FDA 510(k) Submission Details - K262061

510(k) Number K262061 FDA.gov
FDA Decision Cleared Substantially Equivalent - Traditional 510(k) (SESE)
Date Received June 18, 2026
Decision Date July 17, 2026
Days to Decision 29 days
Submission Type Special
Review Panel Orthopedic (OR)
Summary Summary PDF
Third-party Review No - reviewed directly by FDA
Combination Product No
PCCP Authorized No
Regulatory Context
Review time vs. panel average
93d faster than avg
Panel avg: 122d · This submission: 29d
Pathway characteristics
Modification to existing cleared device.

ODP Device Classification - Class 2, Special Controls

Product Code ODP Intervertebral Fusion Device With Bone Graft, Cervical
Device Class Class 2 - Special Controls
CFR Regulation 21 CFR 888.3080
Definition Intended To Stabilize Cervical Spinal Segment To Promote Fusion In Order To Restrict Motion And Decrease Pain Using Bone Graft.
What this classification means

Class II devices require demonstration of substantial equivalence to a legally marketed predicate device. This pathway does not require clinical trials - it relies on engineering equivalence and performance data. Most Orthopedic devices follow this clearance model.

Regulatory Peers - ODP Intervertebral Fusion Device With Bone Graft, Cervical

All 336
Devices cleared under the same product code (ODP) and FDA review panel - the closest regulatory comparables to K262061.
VariLift-C Cervical Interbody Fusion System
K262595 · Wenzel Spine, Inc. · Aug 2026
BluEX Cervical Expandable Cage System
K262489 · L & K Biomed Co., Ltd. · Aug 2026
3d Cage Cervical
K253041 · Fims Co., Ltd. · Jul 2026
C.A. Medical Interbody Fusion System
K254130 · C.A. Medical, LLC · Jul 2026
BluEX Cervical Expandable Cage System
K260840 · L & K Biomed Co., Ltd. · May 2026
OSTEOMNI SPINAL CAGES SYSTEM
K260850 · OSTEOMNI, Inc. · May 2026