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ARTHROSCOPIC ACL CANNULATED DRILLS AND SLEEVES

Page Type
Cleared 510(K)
510(k) Number
K925996
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1993
Days to Decision
109 days
Submission Type
Statement

ARTHROSCOPIC ACL CANNULATED DRILLS AND SLEEVES

Page Type
Cleared 510(K)
510(k) Number
K925996
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/16/1993
Days to Decision
109 days
Submission Type
Statement