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130 MODIFIED INTEGRAL FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984408
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1999
Days to Decision
65 days
Submission Type
Summary

130 MODIFIED INTEGRAL FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984408
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/12/1999
Days to Decision
65 days
Submission Type
Summary