Camber Spine Technologies SPIRA - V Open Matrix Corpectomy Cage
K-Number: K173800 · 2018-02-02
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.