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PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K024086
510(k) Type
Special
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2003
Days to Decision
29 days
Submission Type
Summary

PROPELLER HEAD SMALL CANNULATED SCREW SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K024086
510(k) Type
Special
Applicant
BIOMET ORTHOPEDICS, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
1/9/2003
Days to Decision
29 days
Submission Type
Summary