K241724
- 510(k) number
- K241724
- Device name
- Cytal® Wound Matrix; Cytal® Burn Matrix
- Applicant
- Acell, Inc. MD · US
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2024-07-11
- Date received
- 2024-06-14
- Decision
- Substantially Equivalent
- Clearance type
- Special
- Advisory committee
- Unknown
PDFDownload 510(k) SummaryArchived here · 2.5 MB · U.S. public domain
Also available from FDA: K241724.pdf
Official FDA record: K241724
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.