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SMARTSTITCH SUTURE DEVICE, MODEL OM-8500

Page Type
Cleared 510(K)
510(k) Number
K022229
510(k) Type
Traditional
Applicant
OPUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
58 days
Submission Type
Statement

SMARTSTITCH SUTURE DEVICE, MODEL OM-8500

Page Type
Cleared 510(K)
510(k) Number
K022229
510(k) Type
Traditional
Applicant
OPUS MEDICAL, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/6/2002
Days to Decision
58 days
Submission Type
Statement