FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

ABI Instrument, Creo Electrosurgical System

K Number: K200298 · Decision Jan 5, 2021
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
67
Applicant Total
10
Review Days
334

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Basic Information

Device Name
ABI Instrument, Creo Electrosurgical System
K Number
K200298
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
Creo Medical, Ltd.
Date Received
February 6, 2020
Decision Date
January 5, 2021
Product Code
NEY
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
NEY System, Ablation, Microwave And Accessories

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (NEY), ordered by most recent decision date.

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Other Clearances by Creo Medical, Ltd.

K Number Device Name
K242774 SpydrBlade Flex Instrument (PRD-RG1-001)
K242983 CROMA Electrosurgical Generator (PRD-EMR-050)
K242061 Reusable Interface Cable 1.5 m (PRD-IFC-002)
K230328 Speedboat Flush SB1 Instrument
K223138 AB1 Electrosurgical Instrument, Creo Electrosurgical System
K221672 Creo Electrosurgical System with NP1 Instrument
K200003 NP1 Instrument, Creo Electrosurgical System
K192905 Creo Electrosurgical System with HS1 Hemostasis Accessory
K171983 Creo Medical Electrosurgical System including Speedboat RS2 Surgical Accessory