510(k) K092017 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PIVOTEC LUMBAR INTERBODY FUSION DEVICE (LIFD)
| Applicant | Captiva Spine, Inc., Pleasant Grove UT, US |
| Decision | Substantially Equivalent, Dec 1, 2009 |
| Received | Jul 6, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092017
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.