FDA 510(k) Applications Submitted by APEX SURGICAL, LLC.

FDA 510(k) Number Submission Date Device Name Applicant
K000788 03/10/2000 APEX MODULAR HIP STEM APEX SURGICAL, LLC.
K031110 04/08/2003 APEX MODULAR ACETABULAR CUP APEX SURGICAL, LLC.
K012918 08/30/2001 APEX MODULAR ALUMINA FEMORAL HEAD APEX SURGICAL, LLC.
K043123 11/12/2004 APEX MODULAR HA HIP STEM APEX SURGICAL, LLC.
K003923 12/20/2000 APEX MODULAR ZIRCONIA FEMORAL HEAD APEX SURGICAL, LLC.
K041950 07/20/2004 APEX K2 HIP SYSTEM APEX SURGICAL, LLC.


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