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ASCENT KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011219
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2001
Days to Decision
28 days
Submission Type
Summary

ASCENT KNEE SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K011219
510(k) Type
Special
Applicant
BIOMET, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
5/18/2001
Days to Decision
28 days
Submission Type
Summary