Medical Device Manufacturer · US , Sacramento , CA

Hayes Medical, Inc. - FDA 510(k) Cleared Devices

12 submissions · 11 cleared · Since 1995
12
Total
11
Cleared
0
Denied

Hayes Medical, Inc. has 11 FDA 510(k) cleared orthopedic devices. Based in Sacramento, US.

Historical record: 11 cleared submissions from 1995 to 2007.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Hayes Medical, Inc.
12 devices
1-12 of 12
Cleared Jan 31, 2007
36MM COCR FEMORAL HEAD AND 36MM ACETABULAR INSERT
K070061 · LWJ
Orthopedic · 26d
Cleared Dec 21, 2006
UNISYN HA PLASMA MODULAR HIP
K062383 · LWJ
Orthopedic · 128d
Cleared Apr 28, 2006
CONSENSUS ACETABULAR SHELL SYSTEM
K060635 · LPH
Orthopedic · 49d
Cleared Apr 10, 2003
CONSENSUS HIP SYSTEM, UNISYN HIP SYSTEM
K030151 · LZO
Orthopedic · 85d
Cleared Apr 01, 2003
CONSENSUS UNIPOLAR HEAD, COCR
K030205 · KWL
Orthopedic · 70d
Cleared Jul 24, 2002
CONSENSUS ACETABULAR INSERT, CROSS-LINKED POLYETHYLENE
K021466 · LPH
Orthopedic · 78d
Cleared Apr 15, 2002
CONSENSUS ACETABLAR SHELL, TI COATED
K020153 · LPH
Orthopedic · 89d
Cleared Feb 23, 2001
TRITON HIP SYSTEM
K003649 · LWJ
Orthopedic · 88d
Cleared Aug 07, 2000
CONSENSUS KNEE SYSTEM
K001456 · JWH
Orthopedic · 90d
Cleared Nov 25, 1998
CONSENSUS FEMORAL COMPONENT, POROUS, COCR/TI
K983004 · JWH
Orthopedic · 89d
Cleared Jan 27, 1997
PATIENT SPECIFIC IMPLANT (PSI) HIP FEMORAL COMPONENT
K964395 · LZO
Orthopedic · 84d
Cleared Nov 24, 1995
CORTICELLOUS BONE SCREW
K953198 · HWC
Orthopedic · 141d
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