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OPTILENE MESH LP

Page Type
Cleared 510(K)
510(k) Number
K053158
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
65 days
Submission Type
Summary

OPTILENE MESH LP

Page Type
Cleared 510(K)
510(k) Number
K053158
510(k) Type
Traditional
Applicant
AESCULAP, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/18/2006
Days to Decision
65 days
Submission Type
Summary