510(k) K050924 ยท HWC Screw, Fixation, Bone
MERETE DUOTHREADTM BONE SCREW
| Applicant | Merete Medical GmbH, New York NY, US |
| Decision | Substantially Equivalent, May 27, 2005 |
| Received | Apr 13, 2005 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K050924
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.