510(k) K181357 · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
PATRIOT® Lumbar Spacers, SUSTAIN® Spacers
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Dec 6, 2018 |
| Received | May 22, 2018 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K181357
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.