VEA Align; spineEOS
K-Number: K240582 · 2024-06-25
ApplicantEos Imaging
Decision Date2024-06-25
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
VEA Align; spineEOS is a medical device manufactured by Eos Imaging. It received FDA 510(k) clearance on 2024-06-25 under approval number K240582. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the VEA Align; spineEOS?
VEA Align; spineEOS is a medical device that received FDA 510(k) clearance on 2024-06-25. It is manufactured by Eos Imaging. The 510(k) number is K240582.
When was VEA Align; spineEOS approved by the FDA?
VEA Align; spineEOS received FDA 510(k) clearance on 2024-06-25, under approval number K240582.
What company makes VEA Align; spineEOS?
VEA Align; spineEOS is manufactured by Eos Imaging.
What is the FDA product code for VEA Align; spineEOS?
The FDA product code for VEA Align; spineEOS is QIH.
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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.