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SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K131709
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
115 days
Submission Type
Summary

SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

Page Type
Cleared 510(K)
510(k) Number
K131709
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2013
Days to Decision
115 days
Submission Type
Summary