K243071
- 510(k) number
- K243071
- Device name
- Bovine Dermis Collagen Dermal Matrix
- Applicant
- Collagen Matrix, Inc. NJ · US
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2024-12-19
- Date received
- 2024-09-27
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K243071.pdf
Official FDA record: K243071
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.