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 |