510(k) K980548 ยท GXQ Dura Substitute
DURA-PATCH MODEL DP-XXX
| Applicant | Bridger Biomed, Inc., Bozeman MT, US |
| Decision | Substantially Equivalent, May 13, 1998 |
| Received | Feb 12, 1998 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K980548
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.