Last synced on 11 April 2025 at 11:05 pm

Restrata® MiniMatrix

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223725
510(k) Type
Traditional
Applicant
Acera Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2023
Days to Decision
156 days
Submission Type
Summary

Restrata® MiniMatrix

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K223725
510(k) Type
Traditional
Applicant
Acera Surgical, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2023
Days to Decision
156 days
Submission Type
Summary