
Oratec Interventions, Inc.
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ORATEC INTERVENTIONS MODEL TAC-S MONOPOLAR CAUTERY PROBE (MODIFY) is an FDA 510(k)-cleared medical device (K963157) 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 September 17, 1996. Regulation: 8.