The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zmr Hip System Kwz-prosthesis, Hip, Constrained, Cemented Or Uncemented, Metal/polymer.
Device ID | K113296 |
510k Number | K113296 |
Device Name: | ZMR HIP SYSTEM KWZ-PROSTHESIS, HIP, CONSTRAINED, CEMENTED OR UNCEMENTED, METAL/POLYMER |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Contact | Daniel J Williman |
Correspondent | Daniel J Williman ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Product Code | LPH |
Subsequent Product Code | JDI |
Subsequent Product Code | KWZ |
Subsequent Product Code | LWJ |
Subsequent Product Code | LZO |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-11-08 |
Decision Date | 2012-09-14 |
Summary: | summary |