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SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030

Page Type
Cleared 510(K)
510(k) Number
K993073
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
12/6/1999
Days to Decision
83 days
Submission Type
Summary

SMART SCREW ACL MODELS 237020, 237025, 237030, 238020, 238025, 238030, 239020, 239025, 239030

Page Type
Cleared 510(K)
510(k) Number
K993073
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, LTD.
Country
Finland
FDA Decision
Substantially Equivalent
Decision Date
12/6/1999
Days to Decision
83 days
Submission Type
Summary