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MULTIFIX S KNOTLESS FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131182
510(k) Type
Traditional
Applicant
ARTHOCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2013
Days to Decision
94 days
Submission Type
Summary

MULTIFIX S KNOTLESS FIXATION DEVICE

Page Type
Cleared 510(K)
510(k) Number
K131182
510(k) Type
Traditional
Applicant
ARTHOCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/29/2013
Days to Decision
94 days
Submission Type
Summary