510(k) K023810 ยท JEY Plate, Bone
MODIFICATION TO BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
| Applicant | Bioplate, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Dec 4, 2002 |
| Received | Nov 15, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K023810
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.