The following data is part of a premarket notification filed by Limacorporate S.p.a. with the FDA for Revision Femoral Stem.
| Device ID | K161226 |
| 510k Number | K161226 |
| Device Name: | Revision Femoral Stem |
| Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
| Applicant | LIMACORPORATE S.P.A. VIA NAZIONALE 52 Villanova Di San Daniele, IT 33038 |
| Contact | Emanuele Buttazzoni |
| Correspondent | Stephen Peoples PEOPLE & ASSOCIATES- STEPHEN J. PEOPLES, VMD, MS 411 AUDITORIUM BLVD. Winona Lake, IN 46590 |
| Product Code | LZO |
| Subsequent Product Code | KWY |
| Subsequent Product Code | LPH |
| CFR Regulation Number | 888.3353 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-05-02 |
| Decision Date | 2017-02-10 |
| Summary: | summary |