510(k) K932222

SLT FEMORAL HEAD by Dow Corning Wright — Product Code LZO

K932222 is an FDA 510(k) premarket notification submitted by Dow Corning Wright for the device "SLT FEMORAL HEAD". The FDA issued a decision of Substantially Equivalent on May 27, 1994. 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. Dow Corning Wright has at least 10 other 510(k) clearances on record.