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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 the device name listed in this FDA 510(k) record. The listed applicant is Southern Spine, LLC. It received FDA 510(k) clearance on 2021-11-16 under 510(k) 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. The listed applicant is Southern Spine, LLC. The 510(k) number is K211845.

When did Deploy Expandable Interbody System receive FDA 510(k) clearance?

Deploy Expandable Interbody System received FDA 510(k) clearance on 2021-11-16, under 510(k) number K211845.

Who is the listed applicant for Deploy Expandable Interbody System?

The FDA 510(k) record lists Southern Spine, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Deploy Expandable Interbody System?

The FDA product code for Deploy Expandable Interbody System is MAX.

Related Devices (Code: MAX)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

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