K003979 is an FDA 510(k) clearance for the MEDTRADE PRODUCTS SILICON SCAR MANAGEMENT PAD. This device is classified as a Elastomer, Silicone, For Scar Management (Class I - General Controls, product code MDA).
Submitted by Medtrade Products , Ltd. (Crewe, GB). The FDA issued a Cleared decision on March 19, 2001, 87 days after receiving the submission on December 22, 2000.
This device falls under the General & Plastic Surgery FDA review panel. Regulated under 21 CFR 878.4025.
| 510(k) Number | K003979 FDA.gov |
| FDA Decision | Cleared Substantially Equivalent - Traditional 510(k) (SESE) |
| Date Received | December 22, 2000 |
| Decision Date | March 19, 2001 |
| Days to Decision | 87 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Statement |
| Product Code | MDA — Elastomer, Silicone, For Scar Management |
| Device Class | Class I - General Controls |
| CFR Regulation | 21 CFR 878.4025 |