510(k) K082260 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
INTEGRA CERVICAL AND PETRA PLIF LUMBAR CAGES
| Applicant | Calvary Spine, LLC, Round Rock TX, US |
| Decision | Substantially Equivalent, Oct 17, 2008 |
| Received | Aug 8, 2008 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K082260
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.