510(k) K142707 ยท HWC Screw, Fixation, Bone
AIS Odontoid Fracture Fixation System
| Applicant | Aesculap Implant System, Inc., Center Valley PA, US |
| Decision | Substantially Equivalent, Dec 19, 2014 |
| Received | Sep 22, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K142707
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.