K240277
- 510(k) number
- K240277
- Device name
- MiroDry Wound Matrix
- Applicant
- Reprise Biomedical, Inc. MN · US
- Product code
- KGN — Wound Dressing With Animal-Derived Material(S)
- Decision date
- 2024-03-01
- Date received
- 2024-01-31
- 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: K240277.pdf
Official FDA record: K240277
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.