510(k) K132421 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
AESCULAP PEEK XP SPINAL IMPLANT SYSTEM
| Applicant | Aesculap Implant Systems, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Jan 22, 2014 |
| Received | Aug 5, 2013 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K132421
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.