Restrata® MiniMatrix— 510(k) K223725
Substantially EquivalentAcera Surgical, Inc.
FDA 510(k) clearance K223725 for Restrata® MiniMatrix, Substantially Equivalent on 2023-05-18. Applicant: Acera Surgical, Inc.. Device class: Unclassified.
Clearance details
- Applicant
- Acera Surgical, Inc.
- Product code
- Code QSZ
- Device class
- Unclassified
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Recent devices under product code QSZ
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