The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zimmer Unicompartmental Knee System.
Device ID | K033363 |
510k Number | K033363 |
Device Name: | ZIMMER UNICOMPARTMENTAL KNEE SYSTEM |
Classification | Prosthesis, Knee, Femorotibial, Non-constrained, Cemented, Metal/polymer |
Applicant | ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Contact | Stephen Mckelvey |
Correspondent | Stephen Mckelvey ZIMMER, INC. P.O. BOX 708 Warsaw, IN 46581 -0708 |
Product Code | HSX |
CFR Regulation Number | 888.3520 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2003-10-21 |
Decision Date | 2004-01-16 |
Summary: | summary |