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Adjustable Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K153186
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
86 days
Submission Type
Summary

Adjustable Fixation Device

Page Type
Cleared 510(K)
510(k) Number
K153186
510(k) Type
Traditional
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/28/2016
Days to Decision
86 days
Submission Type
Summary