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SMARTSCREW

Page Type
Cleared 510(K)
510(k) Number
K012001
510(k) Type
Special
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/18/2001
Days to Decision
21 days
Submission Type
Summary

SMARTSCREW

Page Type
Cleared 510(K)
510(k) Number
K012001
510(k) Type
Special
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
7/18/2001
Days to Decision
21 days
Submission Type
Summary