510(k) K171848 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FORTIFY and FORTIFY Integrated Corpectomy Spacers, XPand Corpectomy Spacers, NIKO Corpectomy Spacers, SUSTAIN Spacers, COALITION Spacers, PATRIOT Lumbar Spacers, PATRIOT Cervical Spacers, ALTERA Spacers, RISE Spacers, CALIBER Spacers, ELSA Spacers, LATIS Spacers, MONUMENT Spacers, InterContinental P
| Applicant | Globus Medical, Inc., Audubon PA, US |
| Decision | Substantially Equivalent, Dec 21, 2017 |
| Received | Jun 21, 2017 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K171848
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.