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ARTHROSCOPIC ACL DRILL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K925986
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
99 days
Submission Type
Statement

ARTHROSCOPIC ACL DRILL SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K925986
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/4/1993
Days to Decision
99 days
Submission Type
Statement