510(k) K020221 ยท HRS Plate, Fixation, Bone
IQL BASIC FRAGMENT PLATE SET, IQL BASIC FRAGMENT SCREW SET, IQL SMALL FRAGMENT SET, IQL MINI FRAGMENT SET
| Applicant | Biomet Orthopedics, Inc., Warsaw IN, US |
| Decision | Substantially Equivalent, Apr 2, 2002 |
| Received | Jan 22, 2002 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K020221
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.