Oratec Interventions, Inc.
Oratec Interventions, Inc. holds FDA 510(k) medical device clearances, first cleared 1995, most recent 2002.
Top product codes for Oratec Interventions, Inc.
Recent clearances by Oratec Interventions, Inc.
- K013622 — NUCLEOTOMY INTRADISCAL CATHETER
- K003198 — VULCAN TAC PROBES, MODEL 911XXX
- K003893 — VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X
- K000691 — VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT CHISELS, VULCAN EFLEX LIGAMENT CHISELS
- K992805 — ORATEC ABLATOR-S PROBES (MONOPOLAR ABLATION SUCTION PROBES)
- K994333 — ORA-50 ELECTROTHERMAL SYSTEM AND ACCESSORIES
- K993967 — ORATEC SPINECATH INTRADISCAL CATHETER, MODEL 920002
- K993854 — ORA-50 S AUTOTEMP ELECTROTHERMAL SPINE SYSTEM AND ACCESSORIES
- K991140 — ORATEC INTERVENTIONS VULCAN EAS ELECTROTHERMAL ARTHROSCOPY SYSTEM AND ACCESSORIES
- K991218 — ORATEC BIPOLAR ABLATION PROBES
- K992408 — ELECTROSURGICAL PROBES FAMILY: LIGAMENT CHISELS, MICRO LIGAMENT CHISELS, ABLATOR PROBES
- K991190 — DEFLECTABLE ELECTROSURGICAL PROBES
- K990859 — DEFLECTABLE TAC ELECTROTHERMAL PROBE
- K990474 — ORATEC INTERVENTIONS ORA-50 S PROGRAMMABLE ELECTROTHERMAL SPINE SYSTEM AND ACCESSORIES
- K984185 — MODIFICATION TO TAC-S MONOPOLAR CAUTERY PROBE FAMILY
- K982971 — ORATEC TAC-C, MONOPOLAR CAUTERY PROBE
- K974464 — ORATEC SPINECATH INTRADISCAL CATHETER
- K972358 — ORATEC MODEL ENDOTAC PROBE
- K973158 — ORATEC INTERVENTIONS MODEL ORASTAT MONOPOLAR CAUTERY DEVICE
- K973159 — ORATEC INTERVENTIONS MODEL ORA 40 ELECTROTHERMAL GENERATOR
- K965007 — ORATEC INTERVENTIOUNS ELECTROSURGICAL PROBES
- K964071 — ORATEC INTERVENTIONS MODEL ORA 50 ELECTROTHERMAL GENERATOR
- K963157 — ORATEC INTERVENTIONS MODEL TAC-S MONOPOLAR CAUTERY PROBE (MODIFY)
- K954439 — ORATEC INTERVENTIONS MODEL TAC 1000 MONOPOLAR CAUTERY PROBE
Data sourced from openFDA. This site is unofficial and independent of the FDA.