Last synced on 18 April 2025 at 11:05 pm

All-Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231078
510(k) Type
Traditional
Applicant
Riverpoint Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2023
Days to Decision
171 days
Submission Type
Summary

All-Suture Anchor

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K231078
510(k) Type
Traditional
Applicant
Riverpoint Medical, LLC
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/5/2023
Days to Decision
171 days
Submission Type
Summary