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TRANSTIBIAL ACL DISPOSABLES KIT

Page Type
Cleared 510(K)
510(k) Number
K943943
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
131 days
Submission Type
Statement

TRANSTIBIAL ACL DISPOSABLES KIT

Page Type
Cleared 510(K)
510(k) Number
K943943
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/20/1994
Days to Decision
131 days
Submission Type
Statement