Last synced on 18 April 2025 at 11:05 pm

FASTAK SUTURE ANCHOR (11.7MM)/(7.5MM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971723
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
82 days
Submission Type
Summary

FASTAK SUTURE ANCHOR (11.7MM)/(7.5MM)

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
510(k) Number
K971723
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1997
Days to Decision
82 days
Submission Type
Summary