510(k) K103712 ยท HWC Screw, Fixation, Bone
GRYPHON PEEK DS ANCHOR W/ ORTHOCORD, GRYPHON PEEK ANCHOR W/ ORTHOCORD
| Applicant | Depuy Mitek, A Johnson & Johnson Company, Raynham MA, US |
| Decision | Substantially Equivalent, Mar 11, 2011 |
| Received | Dec 20, 2010 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K103712
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.