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BIOMET CRANIOFACIAL ACRYLIC CEMENT

Page Type
Cleared 510(K)
510(k) Number
K011399
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2003
Days to Decision
728 days
Submission Type
Summary

BIOMET CRANIOFACIAL ACRYLIC CEMENT

Page Type
Cleared 510(K)
510(k) Number
K011399
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/5/2003
Days to Decision
728 days
Submission Type
Summary