The following data is part of a premarket notification filed by Zimmer, Inc with the FDA for Zimmer Biomet Ceramic Heads.
Device ID | K181171 |
510k Number | K181171 |
Device Name: | Zimmer Biomet Ceramic Heads |
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 | Carol Vierling |
Correspondent | Carol Vierling Zimmer, Inc P.O Box 708 Warsaw, IN 46581 -0708 |
Product Code | LZO |
Subsequent Product Code | KWY |
Subsequent Product Code | KWZ |
CFR Regulation Number | 888.3353 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2018-05-02 |
Decision Date | 2019-04-02 |