510(k) K121476 ยท FMF Syringe, Piston
INFILL GRAFT DELIVERY SYSTEM
| Applicant | Pinnacle Spine Group, LLC, Dallas TX, US |
| Decision | Substantially Equivalent, Aug 29, 2012 |
| Received | May 18, 2012 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K121476
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.