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ARTELON SURGICAL SUTURE

Page Type
Cleared 510(K)
510(k) Number
K032160
510(k) Type
Traditional
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2003
Days to Decision
125 days
Submission Type
Summary

ARTELON SURGICAL SUTURE

Page Type
Cleared 510(K)
510(k) Number
K032160
510(k) Type
Traditional
Applicant
ARTIMPLANT AB
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/17/2003
Days to Decision
125 days
Submission Type
Summary