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THERMOFX MESH

Page Type
Cleared 510(K)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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)
PDF
FDA Hosted PDF
* The FDA doesn't provide PDFs for all submissions.
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