Novel Spinal System

FDA 510(k) K081153 · Medyssey Co, Ltd.

Substantially Equivalent

510(k) numberK081153

Submission

Device name
Novel Spinal System
Applicant
Medyssey Co, Ltd.
Santa Fe Springs, CA, US
Received
April 23, 2008
Decision date
January 30, 2009
Decision
Substantially Equivalent (SESE)
Type
Traditional 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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K153404Zavation Spinal SystemMNH · Traditional Zavation, LLC04/21/2016SE
K160020Captiva Spine and CapLOX II/TowerLOX Pedicle Screw SystemMNH · Special Captiva Spine03/02/2016SE
K143013Spinal Inner Fixation SystemMNH · Traditional Changzhou Dingjian Medical Appliance Co., Ltd.12/11/2015SE
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Questions and answers

When was Novel Spinal System cleared by the FDA?

Novel Spinal System (K081153) received a 510(k) decision of Substantially Equivalent on January 30, 2009, 282 days after the submission was received.

What is the product code of K081153?

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