Zodiac Spinal Fixation System

FDA 510(k) K051286 · Alphatec/Nexmed

Substantially Equivalent

510(k) numberK051286

Submission

Device name
Zodiac Spinal Fixation System
Applicant
Alphatec/Nexmed
Carlsbad, CA, US
Received
May 18, 2005
Decision date
June 17, 2005
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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K153404Zavation Spinal SystemMNH · Traditional Zavation, LLC04/21/2016SE
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K143013Spinal Inner Fixation SystemMNH · Traditional Changzhou Dingjian Medical Appliance Co., Ltd.12/11/2015SE
K151695Romeo posterior osteosynthesis systemMNH · Traditional Spineart09/10/2015SE

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Questions and answers

When was Zodiac Spinal Fixation System cleared by the FDA?

Zodiac Spinal Fixation System (K051286) received a 510(k) decision of Substantially Equivalent on June 17, 2005, 30 days after the submission was received.

What is the product code of K051286?

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