510(k) K011032 ยท LYC Bone Grafting Material, Synthetic
SMARTJET BONE GRAFT LIQUID APPLICATOR (SPRAY TIP), MODEL SK/S, SMARTJET BONE GRAFT LIQUID APPLICATOR (DUAL LUMEN CANNULA
| Applicant | Harvest Technologies, Corp., Plymouth MA, US |
| Decision | Substantially Equivalent, Jul 3, 2001 |
| Received | Apr 5, 2001 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K011032
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.