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HEALEY REVISION COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K921139
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1992
Days to Decision
113 days
Submission Type
Statement

HEALEY REVISION COMPONENT SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K921139
510(k) Type
Traditional
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
7/1/1992
Days to Decision
113 days
Submission Type
Statement