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SMARTSCREW MODEL 222006...227510

Page Type
Cleared 510(K)
510(k) Number
K003077
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2001
Days to Decision
205 days
Submission Type
Summary

SMARTSCREW MODEL 222006...227510

Page Type
Cleared 510(K)
510(k) Number
K003077
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/26/2001
Days to Decision
205 days
Submission Type
Summary