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AGC V2 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K984054
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
259 days
Submission Type
Summary

AGC V2 REVISION KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K984054
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/30/1999
Days to Decision
259 days
Submission Type
Summary