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OPUS SMARTSTITCH SUTURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070671
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2007
Days to Decision
25 days
Submission Type
Summary

OPUS SMARTSTITCH SUTURE DEVICE

Page Type
Cleared 510(K)
510(k) Number
K070671
510(k) Type
Special
Applicant
ARTHROCARE CORP.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/6/2007
Days to Decision
25 days
Submission Type
Summary