Last synced on 18 April 2025 at 11:05 pm

ARTHREX SUTURETAK SUTURE ANCHORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140855
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2014
Days to Decision
259 days
Submission Type
Summary

ARTHREX SUTURETAK SUTURE ANCHORS

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K140855
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/18/2014
Days to Decision
259 days
Submission Type
Summary