510(k) K061982 ยท MBP Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)
PLEXUR P
| Applicant | Osteotech, Inc., Eatontown NJ, US |
| Decision | Substantially Equivalent, Feb 7, 2007 |
| Received | Jul 13, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K061982
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.