K960673 is an FDA 510(k) clearance for the OSAP. Classified as Device, Jaw Repositioning (product code LQZ), Class II - Special Controls.
Submitted by Snorefree, Inc. (East Islip, US). The FDA issued a Cleared decision on May 9, 1996 after a review of 79 days - a notably fast clearance cycle.
This device falls under the Dental FDA review panel, regulated under 21 CFR 872.5570 - the FDA dental device regulatory framework. The Traditional 510(k) pathway establishes clearance through substantial equivalence to a legally marketed predicate device, without requiring clinical trial data.
Device pattern: Fast-track predicate clearance. Standard predicate reliance. The short review cycle indicates strong predicate alignment - the FDA found sufficient equivalence without extended technical review.
View all Snorefree, Inc. devices