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ACL TIGHTROPE DOUBLE BUNDLE

Page Type
Cleared 510(K)
510(k) Number
K101837
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2010
Days to Decision
180 days
Submission Type
Summary

ACL TIGHTROPE DOUBLE BUNDLE

Page Type
Cleared 510(K)
510(k) Number
K101837
510(k) Type
Traditional
Applicant
ARTHREX, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/28/2010
Days to Decision
180 days
Submission Type
Summary