Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Deploy Expandable Interbody System

K-Number: K211845 · 2021-11-16

Decision Date2021-11-16
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Deploy Expandable Interbody System is a medical device manufactured by Southern Spine, LLC. It received FDA 510(k) clearance on 2021-11-16 under approval number K211845. The device is classified under product code MAX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

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.