510(k) K113512 ยท JEY Plate, Bone
BIOMET MICROFIXATION MANDIBULAR FRACTURE/ RECONSTRUCTION DEVICES AND PREBENT PLATES SYSTEM
| Applicant | Biomet Microfixation, Jacksonville FL, US |
| Decision | Substantially Equivalent, Jun 29, 2012 |
| Received | Nov 28, 2011 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K113512
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.