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MODULAR HEAD BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K022952
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2002
Days to Decision
88 days
Submission Type
Summary

MODULAR HEAD BONE SCREW

Page Type
Cleared 510(K)
510(k) Number
K022952
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
12/2/2002
Days to Decision
88 days
Submission Type
Summary