510(k) K960362 ยท LZK Implant, Malar
PERMAMESH HYDROXYLAPATITE MATRIX
| Applicant | Ceramed Corp., Lakewood CO, US |
| Decision | Substantially Equivalent, Mar 20, 1996 |
| Received | Jan 25, 1996 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K960362
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.