510(k) K970256 ยท JEY Plate, Bone
INTRAORAL MANDIBULAR DISTRACTION DEVICE
| Applicant | Medicon EG, Washington DC, US |
| Decision | Substantially Equivalent, Mar 11, 1997 |
| Received | Jan 23, 1997 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K970256
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.