Aegis Spine

FDA Filings

This page includes the latest FDA filings for Aegis Spine. Currently, you will find the latest 100 filings for Premarket Notifications, Premarket Applications, De Novo Applications, and GUDID registrations.

Aegis Spine holds import registrations or U.S. agent authorizations in conjunction with the following organizations:

FDA Registration(s)
Registration Number3009790163
FEI Number3009790163
NameAEGIS SPINE
Owner & OperatorAegis Spine
Contact Address9781 S Meridian Blvd Ste 300
Englewood CO 80112 US
Official Correspondent
  • Youngbo Ahn
  • 1-303-7414123-x
Registration Status1
Initial ImporterY
Registration Expiration2020-04-25
Registration Address9781 South Meridian Blvd Suite 300
Englewood, CO 80112 US



FDA Filings

Device
Company
DeviceDate
Aegis Spine
ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System2021-02-16

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