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ACL AVULSION LAG SCREW WITH SHEATH MODEL NUMBER AR-6001

Page Type
Cleared 510(K)
510(k) Number
K981187
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1998
Days to Decision
90 days
Submission Type
Summary

ACL AVULSION LAG SCREW WITH SHEATH MODEL NUMBER AR-6001

Page Type
Cleared 510(K)
510(k) Number
K981187
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1998
Days to Decision
90 days
Submission Type
Summary