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BIOMET SCK KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003296
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2000
Days to Decision
17 days
Submission Type
Summary

BIOMET SCK KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K003296
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
11/6/2000
Days to Decision
17 days
Submission Type
Summary