510(k) K022033 ยท JEY Plate, Bone
STERILE PLATE & SCREW KIT CONFIGURATIONS FOR USE WITH THE BIOPLATE TITANIUM FIXATION SYSTEM
| Applicant | Bioplate, Inc., Washington DC, US |
| Decision | Substantially Equivalent, Jul 19, 2002 |
| Received | Jun 21, 2002 |
| Type | Special |
| FDA record | Open on fda.gov |
Recalls that name K022033
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.