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..
Clearance details
- Applicant
- Acera Surgical, Inc.
- Product code
- Code QSZ
- Advisory panel
- Unknown
- Date received
- Decision date
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Location
- St. Louis, MO, US
Data sourced from openFDA. This site is unofficial and independent of the FDA.