
Oratec Interventions, Inc.
Free shipping on orders over $99 · 30-day returns
ORATEC MODEL ENDOTAC PROBE is an FDA 510(k)-cleared medical device (K972358) manufactured by Oratec Interventions, Inc.. This device is classified under the General, Plastic Surgery specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on January 22, 1998. Regulation: 8.