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

GREEN

K Number: K252060 · Decision Oct 31, 2025
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
64
Applicant Total
5
Review Days
122

Basic Information

Device Name
GREEN
K Number
K252060
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4310
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Phasor Health, LLC
Date Received
July 1, 2025
Decision Date
October 31, 2025
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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