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

AURORA™ Screw System

K Number: K182989 · Decision Dec 18, 2018
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
24
Review Days
50

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Basic Information

Device Name
AURORA™ Screw System
K Number
K182989
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
MiRus, LLC
Date Received
October 29, 2018
Decision Date
December 18, 2018
Product Code
HWC
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWC Screw, Fixation, Bone

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