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

MONTERIS MEDICAL UFO

K Number: K090240 · Decision Aug 6, 2009
Classifications
1
FEI Numbers
250
Registration Numbers
250
Same Product Code
422
Applicant Total
11
Review Days
185

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MONTERIS MEDICAL UFO
K Number
K090240
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4560
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Monteris Medical,
Date Received
February 2, 2009
Decision Date
August 6, 2009
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

Similar 510(k) Clearances

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

View all

Other Clearances by Monteris Medical,

K Number Device Name
K240877 Monteris Medical NeuroBlate System
K231061 NeuroBlate System
K222983 NeuroBlate Fusion-S Software V3.17
K193375 NeuroBlate System
K182036 NeuroBlate System
K173305 NeuroBlate System
K172881 NeuroBlate System
K170724 NeuroBlate System
K132444 ATAMA SYSTEM
K081509 MONTERIS MEDICAL AUTOLITT LASER PROBE
Search all 11 clearances from Monteris Medical, →