Deploy Expandable Interbody System
K-Number: K211845 · 2021-11-16
Device Summary
Frequently Asked Questions
What is the Deploy Expandable Interbody System?
Deploy Expandable Interbody System is a medical device that received FDA 510(k) clearance on 2021-11-16. It is manufactured by Southern Spine, LLC. The 510(k) number is K211845.
When was Deploy Expandable Interbody System approved by the FDA?
Deploy Expandable Interbody System received FDA 510(k) clearance on 2021-11-16, under approval number K211845.
What company makes Deploy Expandable Interbody System?
Deploy Expandable Interbody System is manufactured by Southern Spine, LLC.
What is the FDA product code for Deploy Expandable Interbody System?
The FDA product code for Deploy Expandable Interbody System is MAX.
Related Clinical Trials
Related Devices (Code: MAX)
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.