510(k) K091812 ยท JEY Plate, Bone
FRONTIER DEVICES CRANIOMAXILLOFACIAL, CRANIO CLOSURE, ORTHOGNATHIC, MANDIBLE RECONSTRUCTION AND MESH SYSTEMS
| Applicant | Frontier Devices, Inc., Pelham AL, US |
| Decision | Substantially Equivalent, May 7, 2010 |
| Received | Jun 18, 2009 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K091812
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.