Medical Device Manufacturer · US , Mountain View , CA

Oratec Interventions, Inc. - FDA 510(k) Cleared Devices

24 submissions · 24 cleared · Since 1995

Recent clearances: NUCLEOTOMY INTRADISCAL CATHETER, VULCAN TAC PROBES, MODEL 911XXX, VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL PROBES, MODEL 91000X,91002X,91300X

24
Total
24
Cleared
0
Denied

Oratec Interventions, Inc. has 24 FDA 510(k) cleared general & plastic surgery devices. Based in Mountain View, US.

Historical record: 24 cleared submissions from 1995 to 2002.

Browse the complete list of FDA 510(k) cleared general & plastic surgery devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Oratec Interventions, Inc.

24 devices
1-12 of 24
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