Whiteside Biomechanics, Inc.
Whiteside Biomechanics, Inc. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 2004.
Top product codes for Whiteside Biomechanics, Inc.
Recent clearances by Whiteside Biomechanics, Inc.
- K033313 — QUATRO M FEMORAL COMPONENT
- K012800 — SYMMETRIC UNICOMPARTMENTAL KNEE SYSTEM
- K003618 — WHITESIDE BIOMECHANICS LOW PROFILE STAINLESS STEEL CABLE SYSTEM, MODEL BIO-1-1014
- K993903 — WHITESIDE BIOMECHANICS TITANIUM LOW-PROFILE CABLE, MODEL BIO-1-1013
- K991678 — WHITESIDE BIOMECHANICS SPINAL SYSTEM
- K981238 — BIPOLAR FEMORAL HEAD
- K973261 — WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD
- K964616 — QUATROLOC PLASMA SPRAYED FEMORAL COMPONENT
- K971721 — WHITESIDE BIOMECHANICS, INC. ZIRCONIA CERAMIC FEMORAL HEAD
- K971718 — MICRO-SEAL ACETABULAR SYSTEM
- K964150 — WHITESIDE BIOMECHANICS ZIRCONIA CERAMIC FEMORAL HEAD
- K961625 — QUATROLOC FEMORAL COMPONENT & HEAD
- K961157 — WHITESIDE BIOMECHANICS CANCELLOUS BONE SCREW
Data sourced from openFDA. This site is unofficial and independent of the FDA.