Neodent Implant System- GM Titanium Base for Bridge
K-Number: K192229 · 2019-12-19
Decision Date2019-12-19
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Neodent Implant System- GM Titanium Base for Bridge is a medical device manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2019-12-19 under approval number K192229. 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- GM Titanium Base for Bridge?
Neodent Implant System- GM Titanium Base for Bridge is a medical device that received FDA 510(k) clearance on 2019-12-19. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K192229.
When was Neodent Implant System- GM Titanium Base for Bridge approved by the FDA?
Neodent Implant System- GM Titanium Base for Bridge received FDA 510(k) clearance on 2019-12-19, under approval number K192229.
What company makes Neodent Implant System- GM Titanium Base for Bridge?
Neodent Implant System- GM Titanium Base for Bridge is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..
What is the FDA product code for Neodent Implant System- GM Titanium Base for Bridge?
The FDA product code for Neodent Implant System- GM Titanium Base for Bridge 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.