510(k) K973261

WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD by Whiteside Biomechanics, Inc. — Product Code LZO

K973261 is an FDA 510(k) premarket notification submitted by Whiteside Biomechanics, Inc. for the device "WHITESIDE BIOMECHANICS, INC. CERAMIC UNIPOLAR FEMORAL HEAD". The FDA issued a decision of Substantially Equivalent on November 24, 1997. The device falls under product code LZO (Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented), a Class II device regulated under 21 CFR 888.3353. Whiteside Biomechanics, Inc. has at least 10 other 510(k) clearances on record.