510(k) K151352 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
CONCORDE Bullet Spinal System
| Applicant | Medos International SARL, Le Locle, CH |
| Decision | Substantially Equivalent, Oct 8, 2015 |
| Received | May 20, 2015 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K151352
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.