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FDA 510(k)

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage

K-Number: K173800 · 2018-02-02

Decision Date2018-02-02
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is a medical device manufactured by Camber Spine Technologies. It received FDA 510(k) clearance on 2018-02-02 under approval number K173800. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is a medical device that received FDA 510(k) clearance on 2018-02-02. It is manufactured by Camber Spine Technologies. The 510(k) number is K173800.

When was Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage approved by the FDA?

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage received FDA 510(k) clearance on 2018-02-02, under approval number K173800.

What company makes Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?

Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is manufactured by Camber Spine Technologies.

What is the FDA product code for Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage?

The FDA product code for Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage is MQP.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.