510(k) K102322 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
STINGRAY CERVICAL CAGE; SHARK IMPLANT (PLIF); BULL SHARK IMPLANT(PLIF); TIGER IMPLANT (TLIF); GREAT WHITE IMPLANTS(ALIF)
| Applicant | Omni Surgical, L.P., Round Rock TX, US |
| Decision | Substantially Equivalent, Jan 7, 2011 |
| Received | Aug 17, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K102322
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.