ANAX™ 5.5 Spinal System

FDA 510(k) K162189 · U&I Corporation

Substantially Equivalent

510(k) numberK162189

Submission

Device name
ANAX™ 5.5 Spinal System
Applicant
U&I Corporation
Uijeongbu-Si, KR
Received
August 4, 2016
Decision date
August 30, 2016
Decision
Substantially Equivalent (SESE)
Type
Special 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
MNH – Orthosis, Spondylolisthesis Spinal Fixation
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3070
Specialty
Orthopedic
Implant
Yes

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K151695Romeo posterior osteosynthesis systemMNH · Traditional Spineart09/10/2015SE
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Questions and answers

When was ANAX™ 5.5 Spinal System cleared by the FDA?

ANAX™ 5.5 Spinal System (K162189) received a 510(k) decision of Substantially Equivalent on August 30, 2016, 26 days after the submission was received.

What is the product code of K162189?

The FDA product code is MNH – Orthosis, Spondylolisthesis Spinal Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.