510(k) K800144 ยท JDS Nail, Fixation, Bone
FEMORAL CEMENT RESTRICTOR
| Applicant | Biomet, Inc., Mchenry IL, US |
| Decision | Substantially Equivalent, Feb 19, 1980 |
| Received | Jan 21, 1980 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K800144
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Mar 27, 2017 | Zimmer Biomet, Inc. various polyethylene implants
BIO PLUG 10MM
Product Usage:
Non-weight bearing accessory. Sterile, optional speciality components that are non-bioabsorbable, implantable devices designed to be inse Terminated |
JDS | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.