510(k) K141880 ยท KKY Material, Polytetrafluoroethylene Vitreous Carbon, For Maxillofacial Reconstruction
BIOPOR AOC POROUS POLYETHYLENE, CEREPOR
| Applicant | Ceremed , Inc., Los Angeles CA, US |
| Decision | Substantially Equivalent, Apr 16, 2015 |
| Received | Jul 11, 2014 |
| Type | Traditional |
| FDA record | Open on fda.gov |
Recalls that name K141880
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.