510(k) K072120 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PARAMOUNT INTERVERTEBRAL BODY FUSION DEVICE
| Applicant | Innovative Spinal Technologies, Inc., Mansfield MA, US |
| Decision | Substantially Equivalent, Oct 11, 2007 |
| Received | Aug 1, 2007 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K072120
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.