The following data is part of a premarket notification filed by Zimmer, Inc. with the FDA for Zimmer Distal Radius Plating System.
Device ID | K133246 |
510k Number | K133246 |
Device Name: | ZIMMER DISTAL RADIUS PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ZIMMER, INC. P.O BOX 708 Warsaw, IN 46581 |
Contact | Romil Sheth |
Correspondent | Romil Sheth ZIMMER, INC. P.O BOX 708 Warsaw, IN 46581 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-10-22 |
Decision Date | 2013-12-17 |
Summary: | summary |