Last synced on 27 January 2023 at 11:04 pm

Arthrex LoopLoc Knotless Suture

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212146
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2021
Days to Decision
108 days
Submission Type
Summary

Arthrex LoopLoc Knotless Suture

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K212146
510(k) Type
Traditional
Applicant
Arthrex, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/25/2021
Days to Decision
108 days
Submission Type
Summary