K790987 is an FDA 510(k) clearance for the ZIMMER R TOTAL SHOULDER II. This device is classified as a Prosthesis, Shoulder, Non-constrained, Metal/polymer Cemented (Class II - Special Controls, product code KWT).
Submitted by Zimmer, Inc. (Mchenry, US). The FDA issued a Cleared decision on June 22, 1979, 28 days after receiving the submission on May 25, 1979.
This device falls under the Orthopedic FDA review panel. Regulated under 21 CFR 888.3650.
| 510(k) Number | K790987 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | May 25, 1979 |
| Decision Date | June 22, 1979 |
| Days to Decision | 28 days |
| Submission Type | Traditional |
| Review Panel | Orthopedic (OR) |
| Summary | — |
| Product Code | KWT — Prosthesis, Shoulder, Non-constrained, Metal/polymer Cemented |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 888.3650 |