K243071 is an FDA 510(k) clearance for the Bovine Dermis Collagen Dermal Matrix, a Wound Dressing With Animal-derived Material(s), submitted by Collagen Matrix, Inc. (Oakland, US). The FDA issued a Cleared decision on December 19, 2024, 83 days after receiving the submission on September 27, 2024. This device falls under the General & Plastic Surgery review panel.
| 510(k) Number | K243071 FDA.gov |
| FDA Decision | Cleared SESE |
| Date Received | September 27, 2024 |
| Decision Date | December 19, 2024 |
| Days to Decision | 83 days |
| Submission Type | Traditional |
| Review Panel | General & Plastic Surgery (SU) |
| Summary | Summary PDF |
| Product Code | KGN — Wound Dressing With Animal-derived Material(s) |
| Device Class | — |