Whiteside Biomechanics, Inc. - FDA 510(k) Cleared Devices
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.
13 devices
Cleared
Jul 28, 2004
QUATRO M FEMORAL COMPONENT
Orthopedic
287d
Cleared
May 03, 2002
SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
Orthopedic
255d
Cleared
May 23, 2001
WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL...
Orthopedic
182d
Cleared
Feb 14, 2000
WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
Orthopedic
90d
Cleared
Aug 12, 1999
WHITESIDE BIOMECHANICS SPINAL SYSTEM
Orthopedic
87d
Cleared
Aug 21, 1998
BIPOLAR FEMORAL HEAD
Orthopedic
140d
Cleared
Nov 24, 1997
WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD
Orthopedic
87d
Cleared
Aug 07, 1997
QUATROLOC PLASMA SPRAYED FEMORAL COMPONENT
Orthopedic
287d
Cleared
Jul 30, 1997
WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEAD
Orthopedic
82d
Cleared
Jul 23, 1997
MICRO-SEAL ACETABULAR SYSTEM
Orthopedic
75d
Cleared
Dec 27, 1996
WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEAD
Orthopedic
72d
Cleared
Sep 10, 1996
QUATROLOC FEMORAL COMPONENT & HEAD
Orthopedic
137d
Cleared
May 17, 1996
WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREW
Orthopedic
56d