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BIONX DISTAL RADIUS SCREW

Page Type
Cleared 510(K)
510(k) Number
K974876
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1998
Days to Decision
81 days
Submission Type
Summary

BIONX DISTAL RADIUS SCREW

Page Type
Cleared 510(K)
510(k) Number
K974876
510(k) Type
Traditional
Applicant
BIONX IMPLANTS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/1998
Days to Decision
81 days
Submission Type
Summary