510(k) K111632 ยท FMF Syringe, Piston
INFILL GRAFT DELIVERY SYSTEM
| Applicant | Pinnacle Spine Group, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Aug 11, 2011 |
| Received | Jun 13, 2011 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K111632
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.