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APEX MODULAR ZIRCONIA FEMORAL HEAD

Page Type
Cleared 510(K)
510(k) Number
K003923
510(k) Type
Traditional
Applicant
APEX SURGICAL, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2001
Days to Decision
90 days
Submission Type
Summary

APEX MODULAR ZIRCONIA FEMORAL HEAD

Page Type
Cleared 510(K)
510(k) Number
K003923
510(k) Type
Traditional
Applicant
APEX SURGICAL, LLC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
3/20/2001
Days to Decision
90 days
Submission Type
Summary