FDA 510(k) Application Details - K993967

Device Classification Name	Electrosurgical, Cutting & Coagulation & Accessories   More FDA Info for this Device
510(K) Number	K993967
Device Name	Electrosurgical, Cutting & Coagulation & Accessories
Applicant	ORATEC INTERVENTIONS, INC. 3700 HAVEN CT. MENLO PARK, CA 94025 US Other 510(k) Applications for this Company
Contact	JENNIFER BRENNAN Other 510(k) Applications for this Contact
Regulation Number	878.4400   More FDA Info for this Regulation Number
Classification Product Code	GEI Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	11/23/1999
Decision Date	12/17/1999
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Special
Reviewed By Third Party	N
Expedited Review