Neo Cage System TM
K-Number: K181048 · 2019-01-29
ApplicantNeo Medical SA
Decision Date2019-01-29
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Neo Cage System TM is a medical device manufactured by Neo Medical SA. It received FDA 510(k) clearance on 2019-01-29 under approval number K181048. 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 Neo Cage System TM?
Neo Cage System TM is a medical device that received FDA 510(k) clearance on 2019-01-29. It is manufactured by Neo Medical SA. The 510(k) number is K181048.
When was Neo Cage System TM approved by the FDA?
Neo Cage System TM received FDA 510(k) clearance on 2019-01-29, under approval number K181048.
What company makes Neo Cage System TM?
Neo Cage System TM is manufactured by Neo Medical SA.
What is the FDA product code for Neo Cage System TM?
The FDA product code for Neo Cage System TM is MAX.
Other Devices by Neo Medical SA
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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.