Idys TLIF 3DTi Cages
K-Number: K172465 · 2017-12-15
ApplicantClariance, Sas
Decision Date2017-12-15
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Idys TLIF 3DTi Cages is a medical device manufactured by Clariance, Sas. It received FDA 510(k) clearance on 2017-12-15 under approval number K172465. 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 Idys TLIF 3DTi Cages?
Idys TLIF 3DTi Cages is a medical device that received FDA 510(k) clearance on 2017-12-15. It is manufactured by Clariance, Sas. The 510(k) number is K172465.
When was Idys TLIF 3DTi Cages approved by the FDA?
Idys TLIF 3DTi Cages received FDA 510(k) clearance on 2017-12-15, under approval number K172465.
What company makes Idys TLIF 3DTi Cages?
Idys TLIF 3DTi Cages is manufactured by Clariance, Sas.
What is the FDA product code for Idys TLIF 3DTi Cages?
The FDA product code for Idys TLIF 3DTi Cages is MAX.
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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.