Last synced on 14 November 2025 at 11:06 pm

All-Suture Dual Anchor System

Page Type
Cleared 510(K)
510(k) Number
K250095
510(k) Type
Traditional
Applicant
Suturetech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2025
Days to Decision
234 days
Submission Type
Summary

All-Suture Dual Anchor System

Page Type
Cleared 510(K)
510(k) Number
K250095
510(k) Type
Traditional
Applicant
Suturetech, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/5/2025
Days to Decision
234 days
Submission Type
Summary