Neodent Implant System - Titanium Base for CEREC
K-Number: K160964 · 2016-09-16
Decision Date2016-09-16
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Neodent Implant System - Titanium Base for CEREC is a medical device manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2016-09-16 under approval number K160964. 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 Neodent Implant System - Titanium Base for CEREC?
Neodent Implant System - Titanium Base for CEREC is a medical device that received FDA 510(k) clearance on 2016-09-16. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K160964.
When was Neodent Implant System - Titanium Base for CEREC approved by the FDA?
Neodent Implant System - Titanium Base for CEREC received FDA 510(k) clearance on 2016-09-16, under approval number K160964.
What company makes Neodent Implant System - Titanium Base for CEREC?
Neodent Implant System - Titanium Base for CEREC is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..
What is the FDA product code for Neodent Implant System - Titanium Base for CEREC?
The FDA product code for Neodent Implant System - Titanium Base for CEREC 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.