510(k) K152475 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar
FORZA PTC Spacer System
| Applicant | Orthofix, Inc., Lewisville TX, US |
| Decision | Substantially Equivalent, Jan 14, 2016 |
| Received | Aug 31, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K152475
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.