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APEX KNEE MODULAR TIBIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131472
510(k) Type
Traditional
Applicant
OMNI LIFE SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2013
Days to Decision
139 days
Submission Type
Summary

APEX KNEE MODULAR TIBIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K131472
510(k) Type
Traditional
Applicant
OMNI LIFE SCIENCE, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
10/8/2013
Days to Decision
139 days
Submission Type
Summary