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LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984296
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1999
Days to Decision
79 days
Submission Type
Summary

LATERALIZED INTERGRAL POROUS PRIMARY FEMORAL COMPONENT

Page Type
Cleared 510(K)
510(k) Number
K984296
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
2/18/1999
Days to Decision
79 days
Submission Type
Summary