510(k) K101171 ยท ODP Intervertebral Fusion Device With Bone Graft, Cervical
ORTHOVITA PEEK SPACER
| Applicant | Orthovita, Inc., Malver PA, US |
| Decision | Substantially Equivalent, Jan 25, 2011 |
| Received | Apr 26, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K101171
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.