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MODIFICATION TO FLUOROTEX II SURGICAL MESH

Page Type
Cleared 510(K)
510(k) Number
K003917
510(k) Type
Traditional
Applicant
BRIDGER BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2001
Days to Decision
38 days
Submission Type
Summary

MODIFICATION TO FLUOROTEX II SURGICAL MESH

Page Type
Cleared 510(K)
510(k) Number
K003917
510(k) Type
Traditional
Applicant
BRIDGER BIOMED, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/26/2001
Days to Decision
38 days
Submission Type
Summary