The following data is part of a premarket notification filed by Zimmer, Inc with the FDA for Avenir Complete Hip System.
Device ID | K182048 |
510k Number | K182048 |
Device Name: | Avenir Complete Hip System |
Classification | Prosthesis, Hip, Semi-constrained, Metal/ceramic/polymer, Cemented Or Non-porous, Uncemented |
Applicant | Zimmer, Inc P.O. Box 708 Warsaw, IN 46581 -0708 |
Contact | Rebecca D Noftz |
Correspondent | Neha Sreenath Zimmer GmbH Sulzerallee 8 Winterthur, CH 8404 |
Product Code | LZO |
Subsequent Product Code | KWY |
Subsequent Product Code | KWZ |
Subsequent Product Code | LWJ |
Subsequent Product Code | MEH |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-07-31 |
Decision Date | 2018-12-07 |
Summary: | summary |