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FDA 510(k) Applications Submitted by MICHAEL KWAN
FDA 510(k) Number
Submission Date
Device Name
Applicant
K972358
06/25/1997
ORATEC MODEL ENDOTAC PROBE
ORATEC INTERVENTIONS, INC.
K973158
08/22/1997
ORATEC INTERVENTIONS MODEL ORASTAT MONOPOLAR CAUTERY DEVICE
ORATEC INTERVENTIONS, INC.
K973159
08/22/1997
ORATEC INTERVENTIONS MODEL ORA 40 ELECTROTHERMAL GENERATOR
ORATEC INTERVENTIONS, INC.
K974464
11/26/1997
ORATEC SPINECATH INTRADISCAL CATHETER
ORATEC INTERVENTIONS, INC.
K965007
12/16/1996
ORATEC INTERVENTIOUNS ELECTROSURGICAL PROBES
ORATEC INTERVENTIONS, INC.
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