ArgenIS Titanium Abutments
K-Number: K172430 · 2018-05-18
ApplicantArgen Corporation
Decision Date2018-05-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
ArgenIS Titanium Abutments is a medical device manufactured by Argen Corporation. It received FDA 510(k) clearance on 2018-05-18 under approval number K172430. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the ArgenIS Titanium Abutments?
ArgenIS Titanium Abutments is a medical device that received FDA 510(k) clearance on 2018-05-18. It is manufactured by Argen Corporation. The 510(k) number is K172430.
When was ArgenIS Titanium Abutments approved by the FDA?
ArgenIS Titanium Abutments received FDA 510(k) clearance on 2018-05-18, under approval number K172430.
What company makes ArgenIS Titanium Abutments?
ArgenIS Titanium Abutments is manufactured by Argen Corporation.
What is the FDA product code for ArgenIS Titanium Abutments?
The FDA product code for ArgenIS Titanium Abutments is NHA.
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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.