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OPTILENE MESH

Page Type
Cleared 510(K)
510(k) Number
K061704
510(k) Type
Special
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2006
Days to Decision
33 days
Submission Type
Summary

OPTILENE MESH

Page Type
Cleared 510(K)
510(k) Number
K061704
510(k) Type
Special
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/19/2006
Days to Decision
33 days
Submission Type
Summary