FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

ORATEC BIPOLAR ABLATION PROBES

K Number: K991218 · Decision Sep 13, 1999
Classifications
1
FEI Numbers
823
Registration Numbers
823
Same Product Code
2306
Applicant Total
24
Review Days
154

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Basic Information

Device Name
ORATEC BIPOLAR ABLATION PROBES
K Number
K991218
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4400
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Oratec Interventions, Inc.
Date Received
April 12, 1999
Decision Date
September 13, 1999
Product Code
GEI
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GEI Electrosurgical, Cutting & Coagulation & Accessories

Similar 510(k) Clearances

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Other Clearances by Oratec Interventions, Inc.

K Number Device Name
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
K992408 ELECTROSURGICAL PROBES FAMILY: LIGAMENT CHISELS, MICRO LIGAMENT CHISELS, ABLATOR PROBES
Search all 24 clearances from Oratec Interventions, Inc. →