K261224
- 510(k) number
- K261224
- Device name
- MatriDerm
- Applicant
- Medskin Solutions Dr. Suwelack AG DE
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2026-05-14
- Date received
- 2026-04-14
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.6 MB · U.S. public domain
Also available from FDA: K261224.pdf
Official FDA record: K261224
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.