spineEOS
K-Number: K232086 · 2023-10-24
ApplicantEos Imaging
Decision Date2023-10-24
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent
Device Summary
spineEOS is a medical device manufactured by Eos Imaging. It received FDA 510(k) clearance on 2023-10-24 under approval number K232086. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the spineEOS?
spineEOS is a medical device that received FDA 510(k) clearance on 2023-10-24. It is manufactured by Eos Imaging. The 510(k) number is K232086.
When was spineEOS approved by the FDA?
spineEOS received FDA 510(k) clearance on 2023-10-24, under approval number K232086.
What company makes spineEOS?
spineEOS is manufactured by Eos Imaging.
What is the FDA product code for spineEOS?
The FDA product code for spineEOS is LLZ.
Related Clinical Trials
Other Devices by Eos Imaging
Related Devices (Code: LLZ)
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.