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NUGEN FX SCREW

Page Type
Cleared 510(K)
510(k) Number
K023022
510(k) Type
Special
Applicant
BIONX IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2002
Days to Decision
23 days
Submission Type
Summary

NUGEN FX SCREW

Page Type
Cleared 510(K)
510(k) Number
K023022
510(k) Type
Special
Applicant
BIONX IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/4/2002
Days to Decision
23 days
Submission Type
Summary