510(k) K002879 ยท JEY Plate, Bone
MODIFICATION TO BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
| Applicant | Bioplate, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Oct 5, 2000 |
| Received | Sep 15, 2000 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K002879
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.