510(k) K022890 ยท JEY Plate, Bone
MODIFIED SCREW DESIGNS FOR USE WITH THE BIOPLATE RIGID FIXATION BONE PLATING SYSTEM FOR CRANIOMAXILLOFACIAL SURGERY
| Applicant | Bioplate, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Sep 6, 2002 |
| Received | Aug 30, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022890
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.