Idys ALIF ZP 3DTi
K-Number: K200920 · 2020-05-29
ApplicantClariance, Sas
Decision Date2020-05-29
Product CodeMAX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Idys ALIF ZP 3DTi is a medical device manufactured by Clariance, Sas. It received FDA 510(k) clearance on 2020-05-29 under approval number K200920. 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 ALIF ZP 3DTi?
Idys ALIF ZP 3DTi is a medical device that received FDA 510(k) clearance on 2020-05-29. It is manufactured by Clariance, Sas. The 510(k) number is K200920.
When was Idys ALIF ZP 3DTi approved by the FDA?
Idys ALIF ZP 3DTi received FDA 510(k) clearance on 2020-05-29, under approval number K200920.
What company makes Idys ALIF ZP 3DTi?
Idys ALIF ZP 3DTi is manufactured by Clariance, Sas.
What is the FDA product code for Idys ALIF ZP 3DTi?
The FDA product code for Idys ALIF ZP 3DTi 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.