510(k) K060248 ยท HWC Screw, Fixation, Bone
ULTRATINE TRANSBLEPH
| Applicant | Coapt Systems, Inc., Palo Alto CA, US |
| Decision | Substantially Equivalent, Jun 12, 2006 |
| Received | Jan 31, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K060248
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.