510(k) K130506 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
IMSE P-TLIF
| Applicant | Institute of Musculoskeletal Science & Education, Newtown Square PA, US |
| Decision | Substantially Equivalent, May 13, 2013 |
| Received | Feb 27, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K130506
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.