510(k) K151056 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Aesculap T-Space PEEK and XP Spinal System
| Applicant | Aesculap Implant Systems, LLC, Center Valley PA, US |
| Decision | Substantially Equivalent, Aug 13, 2015 |
| Received | Apr 20, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K151056
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.