Oratec Interventions, Inc. - FDA 510(k) Cleared Devices
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.
24 devices
Cleared
Jan 31, 2002
NUCLEOTOMY INTRADISCAL CATHETER
General & Plastic Surgery
87d
Cleared
Aug 29, 2001
VULCAN TAC PROBES, MODEL 911XXX
Orthopedic
321d
Cleared
Mar 01, 2001
VULCAN ABLATOR ELECTROSURGICAL PROBES, VULCAN LIGAMENT CHISEL ELECTROSURGICAL...
Orthopedic
73d
Cleared
May 04, 2000
VULCAN ELECTROSURGICAL PROBES: VULCAN MICRO LIGAMENT CHISELS, VULCAN LIGAMENT...
Orthopedic
65d
Cleared
Feb 04, 2000
ORATEC ABLATOR-S PROBES (MONOPOLAR ABLATION SUCTION PROBES)
General & Plastic Surgery
168d
Cleared
Jan 18, 2000
ORA-50 ELECTROTHERMAL SYSTEM AND ACCESSORIES
General & Plastic Surgery
26d
Cleared
Dec 17, 1999
ORATEC SPINECATH INTRADISCAL CATHETER, MODEL 920002
General & Plastic Surgery
24d
Cleared
Dec 06, 1999
ORA-50 S AUTOTEMP ELECTROTHERMAL SPINE SYSTEM AND ACCESSORIES
General & Plastic Surgery
21d
Cleared
Oct 25, 1999
ORATEC INTERVENTIONS VULCAN EAS ELECTROTHERMAL ARTHROSCOPY SYSTEM AND...
General & Plastic Surgery
203d
Cleared
Sep 13, 1999
ORATEC BIPOLAR ABLATION PROBES
General & Plastic Surgery
154d
Cleared
Jul 30, 1999
ELECTROSURGICAL PROBES FAMILY: LIGAMENT CHISELS, MICRO LIGAMENT CHISELS,...
General & Plastic Surgery
10d
Cleared
Jun 23, 1999
DEFLECTABLE ELECTROSURGICAL PROBES
General & Plastic Surgery
76d