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

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