K142403 is an FDA 510(k) clearance for the Anatomical Shoulder System/Anatomical Shoulder Domelock System/Anatomical Shoulder Fracture System. This device is classified as a Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented (Class II - Special Controls, product code KWS).
Submitted by Zimmer GmbH (Winterthur, CH). The FDA issued a Cleared decision on November 24, 2014, 89 days after receiving the submission on August 27, 2014.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3660.
| 510(k) Number | K142403 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | August 27, 2014 |
| Decision Date | November 24, 2014 |
| Days to Decision | 89 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | Summary PDF |
| Product Code | KWS — Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3660 |