
Oratec Interventions, Inc.
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ORATEC SPINECATH INTRADISCAL CATHETER, MODEL 920002 is an FDA 510(k)-cleared medical device (K993967) 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 December 16, 1999. Regulation: 8.