Last synced on 14 November 2025 at 11:06 pm

ARTHREX SPEEDCINCH

Page Type
Cleared 510(K)
510(k) Number
K132043
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2013
Days to Decision
29 days
Submission Type
Summary

ARTHREX SPEEDCINCH

Page Type
Cleared 510(K)
510(k) Number
K132043
510(k) Type
Special
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/31/2013
Days to Decision
29 days
Submission Type
Summary