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CANNULATED SMARTSCREW MODELS 224540C, 224570C

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