K921581 is an FDA 510(k) clearance for the CHIN WAFER. This device is classified as a Prosthesis, Chin, Internal (Class II - Special Controls, product code FWP).
Submitted by Implantech Associates, Inc. (Washington, US). The FDA issued a Cleared decision on May 6, 1992, 34 days after receiving the submission on April 2, 1992.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.3550.
| 510(k) Number | K921581 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | April 02, 1992 |
| Decision Date | May 06, 1992 |
| Days to Decision | 34 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | FWP - Prosthesis, Chin, Internal |
| Device Class | Class II - Special Controls |
| CFR Regulation | 21 CFR 878.3550 |