510(k) K980817 ยท MQV Filler, Bone Void, Calcium Compound
PRO OSTEON IMPLANT 500R RESORBABLE BONE GRAFT SUBSTITUTE MODEL NUMBERS 5RG05, 5RG10, 5RG15, 5G15L, 5RG20, 5RG30, 5RG30L
| Applicant | Interpore Intl., Irvine CA, US |
| Decision | Substantially Equivalent, Sep 25, 1998 |
| Received | Mar 3, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980817
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.