Medical Device Manufacturer · US , Taunton , MA

Apex Surgical, LLC - FDA 510(k) Cleared Devices

6 submissions · 6 cleared · Since 2000
6
Total
6
Cleared
0
Denied

Apex Surgical, LLC has 6 FDA 510(k) cleared medical devices. Based in Taunton, US.

Historical record: 6 cleared submissions from 2000 to 2005. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Apex Surgical, LLC Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Apex Surgical, LLC
6 devices
1-6 of 6
Cleared Feb 10, 2005
APEX MODULAR HA HIP STEM
K043123 · LPH
Orthopedic · 90d
Cleared Dec 21, 2004
APEX K2 HIP SYSTEM
K041950 · LPH
Orthopedic · 154d
Cleared May 22, 2003
APEX MODULAR ACETABULAR CUP
K031110 · LPH
Orthopedic · 44d
Cleared Nov 27, 2001
APEX MODULAR ALUMINA FEMORAL HEAD
K012918 · LZO
Orthopedic · 89d
Cleared Mar 20, 2001
APEX MODULAR ZIRCONIA FEMORAL HEAD
K003923 · LZO
Orthopedic · 90d
Cleared Aug 04, 2000
APEX MODULAR HIP STEM
K000788 · LPH
Orthopedic · 147d
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