Last synced on 14 November 2025 at 11:06 pm

ASCENT KNEE REVISION FEMORAL STEM

Page Type
Cleared 510(K)
510(k) Number
K001010
510(k) Type
Special
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2000
Days to Decision
29 days
Submission Type
Summary

ASCENT KNEE REVISION FEMORAL STEM

Page Type
Cleared 510(K)
510(k) Number
K001010
510(k) Type
Special
Applicant
Biomet, Inc.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
4/27/2000
Days to Decision
29 days
Submission Type
Summary