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FDA 510(k)

Neodent Implant System - CM Pro PEEK Abutment

K-Number: K170080 · 2017-11-02

Decision Date2017-11-02
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Neodent Implant System - CM Pro PEEK Abutment is a medical device manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. It received FDA 510(k) clearance on 2017-11-02 under approval number K170080. 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 - CM Pro PEEK Abutment?

Neodent Implant System - CM Pro PEEK Abutment is a medical device that received FDA 510(k) clearance on 2017-11-02. It is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A.. The 510(k) number is K170080.

When was Neodent Implant System - CM Pro PEEK Abutment approved by the FDA?

Neodent Implant System - CM Pro PEEK Abutment received FDA 510(k) clearance on 2017-11-02, under approval number K170080.

What company makes Neodent Implant System - CM Pro PEEK Abutment?

Neodent Implant System - CM Pro PEEK Abutment is manufactured by Jjgc Industria E Comercio DE Materiais Dentarios S.A..

What is the FDA product code for Neodent Implant System - CM Pro PEEK Abutment?

The FDA product code for Neodent Implant System - CM Pro PEEK Abutment is NHA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.