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SINUS DILATION SYSTEM WITH CANNULATED INSTRUMENT

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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