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APEX KNEE MODULAR TIBIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101994
510(k) Type
Traditional
Applicant
OMNLIFE SCIENCE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2010
Days to Decision
75 days
Submission Type
Summary

APEX KNEE MODULAR TIBIA SYSTEM

Page Type
Cleared 510(K)
510(k) Number
K101994
510(k) Type
Traditional
Applicant
OMNLIFE SCIENCE
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
9/28/2010
Days to Decision
75 days
Submission Type
Summary