Magic UCLA Abutment System
K-Number: K202418 · 2020-12-03
ApplicantInnobiosurg Co., Ltd.
Decision Date2020-12-03
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Magic UCLA Abutment System is a medical device manufactured by Innobiosurg Co., Ltd.. It received FDA 510(k) clearance on 2020-12-03 under approval number K202418. 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 Magic UCLA Abutment System?
Magic UCLA Abutment System is a medical device that received FDA 510(k) clearance on 2020-12-03. It is manufactured by Innobiosurg Co., Ltd.. The 510(k) number is K202418.
When was Magic UCLA Abutment System approved by the FDA?
Magic UCLA Abutment System received FDA 510(k) clearance on 2020-12-03, under approval number K202418.
What company makes Magic UCLA Abutment System?
Magic UCLA Abutment System is manufactured by Innobiosurg Co., Ltd..
What is the FDA product code for Magic UCLA Abutment System?
The FDA product code for Magic UCLA Abutment System is NHA.
Related Clinical Trials
Other Devices by Innobiosurg Co., Ltd.
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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.