510(k) K092483 ยท GDW Staple, Implantable
BARD PERMAFIX FIXATION SYSTEM, MODEL 0113012, 0113014, 0113016, 0116018
| Applicant | C.R. Bard, Inc., Warwick RI, US |
| Decision | Substantially Equivalent, Dec 18, 2009 |
| Received | Aug 13, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K092483
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.