Medical Device Manufacturer · US , Creve Coeur , MO

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

13 submissions · 12 cleared · Since 1996

Recent clearances: WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013, WHITESIDE BIOMECHANICS SPINAL SYSTEM, BIPOLAR FEMORAL HEAD

13

Total

12

Cleared

0

Denied

FDA 510(k) Regulatory Record - Whiteside Biomechanics, Inc. Orthopedic ✕

13 devices

1-12 of 13

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