Facilis Spinal System
K-Number: K161231 · 2017-01-23
Device Summary
Frequently Asked Questions
What is the Facilis Spinal System?
Facilis Spinal System is a medical device that received FDA 510(k) clearance on 2017-01-23. It is manufactured by Baui Biotech Co., Ltd.. The 510(k) number is K161231.
When was Facilis Spinal System approved by the FDA?
Facilis Spinal System received FDA 510(k) clearance on 2017-01-23, under approval number K161231.
What company makes Facilis Spinal System?
Facilis Spinal System is manufactured by Baui Biotech Co., Ltd..
What is the FDA product code for Facilis Spinal System?
The FDA product code for Facilis Spinal System is NKB.
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Related PubMed Literature
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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.