510(k) K040740 ยท HWC Screw, Fixation, Bone
ENDOTINE TRANSBLEPH DEVICE
| Applicant | Coapt Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, May 10, 2004 |
| Received | Mar 22, 2004 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K040740
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.