510(k) K062421 ยท MRD Mammary Sizer
MENTOR RESTERILIZABLE GEL BREAST IMPLANT SIZER
| Applicant | Mentor Corporation, Santa Barbara CA, US |
| Decision | Substantially Equivalent, Oct 10, 2006 |
| Received | Aug 18, 2006 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K062421
| Date | Firm and product | Code | Linked 510(k) |
|---|---|---|---|
| Jan 13, 2015 | Mentor Texas, LP. MENTOR MemoryGel Resterilizable Gel Sizer Moderate Plus Profile STERILE. Breast prosthesis sizer. Terminated |
MRD | None listed |
Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.