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

EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL

K Number: K080802 · Decision Apr 30, 2008
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
64
Applicant Total
60
Review Days
40

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Basic Information

Device Name
EMAX 2 PLUS SYSTEM, MODEL EMAX 2 PLUS MOTOR, EMAX 2 CONSOLE>FIRMWARE UPGRADE, EMAX 2 FP FOOT PEDAL
K Number
K080802
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
882.4310
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
The Anspach Effort, Inc.
Date Received
March 21, 2008
Decision Date
April 30, 2008
Product Code
HBE
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
HBE Drills, Burrs, Trephines & Accessories (Simple, Powered)

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