SYNTHES 9USA) ALVEOLAR RIDGE DISTRACTOR

SYNTHES 9USA) ALVEOLAR RIDGE DISTRACTOR is an FDA 510(k)-cleared medical device (K043555) manufactured by Synthes (Usa). This device is classified under the Dental specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on April 11, 2005. Regulation: 8.