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THERMOFX MESH

Page Type
Cleared 510(K)
510(k) Number
K003757
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
2/7/2001
Days to Decision
63 days
Submission Type
Summary

THERMOFX MESH

Page Type
Cleared 510(K)
510(k) Number
K003757
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
2/7/2001
Days to Decision
63 days
Submission Type
Summary