510(k) K161407 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
Ascential IBD PEEKc Spacer
| Applicant | Stryker Spine, Allendale NJ, US |
| Decision | Substantially Equivalent, Jul 15, 2016 |
| Received | May 20, 2016 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K161407
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.