510(k) K011380 ยท JEY Plate, Bone
MODIFICATION TO THE BIOPLATE BIOCLIP CRANIOTOMY FIXATION SYSTEM
| Applicant | Bioplate, Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, May 14, 2001 |
| Received | May 7, 2001 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K011380
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.