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SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE

Page Type
Cleared 510(K)
510(k) Number
K121306
510(k) Type
Traditional
Applicant
ARTHOCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
72 days
Submission Type
Summary

SMARTSTITCH M-CONNECTOR ULTRA SMARTSTITCH SUTURE DEVICE HANDLE SMARTSTITCH SUTURE DEVICE HANDLE

Page Type
Cleared 510(K)
510(k) Number
K121306
510(k) Type
Traditional
Applicant
ARTHOCARE CORPORATION
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/12/2012
Days to Decision
72 days
Submission Type
Summary