510(k) K262061 · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Tritanium® C Anterior Cervical Cage; 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
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 17, 2026 |
| Received | Jun 18, 2026 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K262061
No recall in the FDA data names this 510(k).
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.