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PEGGED ACETABULAR COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K970501
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1997
Days to Decision
79 days
Submission Type
Summary

PEGGED ACETABULAR COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K970501
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/30/1997
Days to Decision
79 days
Submission Type
Summary