The following data is part of a premarket notification filed by Zimmer Gmbh with the FDA for Anatomical Shoulder System/anatomical Shoulder Domelock System/anatomical Shoulder Fracture System.
Device ID | K142403 |
510k Number | K142403 |
Device Name: | Anatomical Shoulder System/Anatomical Shoulder Domelock System/Anatomical Shoulder Fracture System |
Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
Applicant | ZIMMER GMBH SULZERALLEE 8 Winterthur, CH 8404 |
Contact | Roberto Tommasini |
Correspondent | Annemie Rehor Kausch ZIMMER GMBH SULZERALLEE 8 Winterthur, CH 8404 |
Product Code | KWS |
Subsequent Product Code | HSD |
Subsequent Product Code | KWT |
Subsequent Product Code | PHX |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-08-27 |
Decision Date | 2014-11-24 |
Summary: | summary |