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SURGICRAFT SURGICAL MESH SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072370
510(k) Type
Traditional
Applicant
SURGICRAFT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2008
Days to Decision
336 days
Submission Type
Summary

SURGICRAFT SURGICAL MESH SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K072370
510(k) Type
Traditional
Applicant
SURGICRAFT LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/24/2008
Days to Decision
336 days
Submission Type
Summary