Medical Device Manufacturer · US , Creve Coeur , MO

Whiteside Biomechanics, Inc. - FDA 510(k) Cleared Devices

13 submissions · 12 cleared · Since 1996
13
Total
12
Cleared
0
Denied

Whiteside Biomechanics, Inc. has 12 FDA 510(k) cleared orthopedic devices. Based in Creve Coeur, US.

Historical record: 12 cleared submissions from 1996 to 2004.

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 - Whiteside Biomechanics, Inc.
13 devices
1-12 of 13
Cleared Jul 28, 2004
QUATRO M FEMORAL COMPONENT
K033313 · LWJ
Orthopedic · 287d
Cleared May 03, 2002
SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
K012800 · HRY
Orthopedic · 255d
Cleared May 23, 2001
WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL...
K003618 · NDD
Orthopedic · 182d
Cleared Feb 14, 2000
WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
K993903 · JDQ
Orthopedic · 90d
Cleared Aug 12, 1999
WHITESIDE BIOMECHANICS SPINAL SYSTEM
K991678 · KWQ
Orthopedic · 87d
Cleared Aug 21, 1998
BIPOLAR FEMORAL HEAD
K981238 · KWY
Orthopedic · 140d
Cleared Nov 24, 1997
WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD
K973261 · LZO
Orthopedic · 87d
Cleared Aug 07, 1997
QUATROLOC PLASMA SPRAYED FEMORAL COMPONENT
K964616 · LPH
Orthopedic · 287d
Cleared Jul 30, 1997
WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEAD
K971721 · LZO
Orthopedic · 82d
Cleared Jul 23, 1997
MICRO-SEAL ACETABULAR SYSTEM
K971718 · LPH
Orthopedic · 75d
Cleared Dec 27, 1996
WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEAD
K964150 · LZO
Orthopedic · 72d
Cleared Sep 10, 1996
QUATROLOC FEMORAL COMPONENT & HEAD
K961625 · LPH
Orthopedic · 137d
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