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

L300 Go System

K Number: K190285 · Decision Mar 14, 2019
Classifications
1
FEI Numbers
38
Registration Numbers
38
Same Product Code
60
Applicant Total
13
Review Days
31

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Basic Information

Device Name
L300 Go System
K Number
K190285
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.5810
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Bioness, Inc.
Date Received
February 11, 2019
Decision Date
March 14, 2019
Product Code
GZI
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

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

Product Code Device Name
GZI Stimulator, Neuromuscular, External Functional

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Other Clearances by Bioness, Inc.

K Number Device Name
K211965 StimRouter Neuromodulation System
K200482 StimRouter Neuromodulation System
K200262 L100 Go System
K190047 StimRouter Neuromodulation System
K191587 L360 Thigh System
K173682 L300 Go System
K162407 L300 Go System
K142432 StimRouter Lead Kit/StimRouter Surgical Tool Kit/StimRouter Clinician Kit/StimRouter User Kit
K123636 H200 WIRELESS HAND REHABILITATION SYSTEM WITH OPTIONAL INTELLI-CONNECT EARPIECE TRIGGERING DEVICE
K122784 NESS L300 SYSTEM KIT, LEF MODEL LG3-5100; NESS L300 SYSTEM KIT, RIGHT MODEL LG3-5000; SMALL NESS L300 SYSTEM KIT, RIGHT
Search all 13 clearances from Bioness, Inc. →