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CANNULATED SMARTSCREW MODELS 224540C, 224570C

Page Type
Cleared 510(K)
510(k) Number
K992947
510(k) Type
Special
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
9/21/1999
Days to Decision
20 days
Submission Type
Summary

CANNULATED SMARTSCREW MODELS 224540C, 224570C

Page Type
Cleared 510(K)
510(k) Number
K992947
510(k) Type
Special
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
9/21/1999
Days to Decision
20 days
Submission Type
Summary