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

SYMBIS Surgical System

K Number: K143420 · Decision Oct 30, 2015
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
14
Review Days
336

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Basic Information

Device Name
SYMBIS Surgical System
K Number
K143420
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Imris, Inc.
Date Received
November 28, 2014
Decision Date
October 30, 2015
Product Code
HAW
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
HAW Neurological Stereotaxic Instrument

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Other Clearances by Imris, Inc.

K Number Device Name
K141950 HFD100 ROCKER ARM ACCESSORY
K133692 IMRI 1.5T AND IMRI 3T S
K130224 ICT
K123091 VISIUS WIRELESS COILS, 1.5T/ VISIUS WIRELESS COILS, 3T
K121997 IMRIS ONCOLOGY PACKAGE
K113748 IMRIS MR/X-RAY HEAD FIXATION DEVICE (HFD)
K103493 HEAD FIATION DEVICE (HFD 100)
K103506 1.5T HEAD COIL (HC150), 3T HEAD COIL (HC300)
K101813 IMRX SYSTEM V1 AND IMRISNV/IMRISCARDIO
K091166 IMRX
Search all 14 clearances from Imris, Inc. →