510(k) K063584 ยท HWC Screw, Fixation, Bone
STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937
| Applicant | Regeneration Technologies, Inc., Alachua FL, US |
| Decision | Substantially Equivalent, May 9, 2007 |
| Received | Dec 1, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K063584
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.