Last synced on 14 November 2025 at 11:06 pm

ARTHREX BIOCOMPOSITE SUTURETAK

Page Type
Cleared 510(K)
510(k) Number
K110660
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2011
Days to Decision
24 days
Submission Type
Summary

ARTHREX BIOCOMPOSITE SUTURETAK

Page Type
Cleared 510(K)
510(k) Number
K110660
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/31/2011
Days to Decision
24 days
Submission Type
Summary