510(k) K150673 ยท OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
SYNFIX Evolution Secured Spacer System
| Applicant | Synthes (USA) Products, LLC, Raynham MA, US |
| Decision | Substantially Equivalent, Aug 21, 2015 |
| Received | Mar 16, 2015 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K150673
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.