510(k) K132775

PONTO PLUS AND PONTO PLUS POWER by Oticon Medical AB — Product Code LXB

K132775 is an FDA 510(k) premarket notification submitted by Oticon Medical AB for the device "PONTO PLUS AND PONTO PLUS POWER". The FDA issued a decision of Substantially Equivalent on December 9, 2013. The device falls under product code LXB (Hearing Aid, Bone Conduction), a Class II device regulated under 21 CFR 874.3302. Oticon Medical AB has at least 10 other 510(k) clearances on record.