Multi-unit Abutment, Multi-unit Angled Abutment
K-Number: K203808 · 2021-10-20
ApplicantMegagen Implant Co., Ltd.
Decision Date2021-10-20
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Multi-unit Abutment, Multi-unit Angled Abutment is a medical device manufactured by Megagen Implant Co., Ltd.. It received FDA 510(k) clearance on 2021-10-20 under approval number K203808. 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 Multi-unit Abutment, Multi-unit Angled Abutment?
Multi-unit Abutment, Multi-unit Angled Abutment is a medical device that received FDA 510(k) clearance on 2021-10-20. It is manufactured by Megagen Implant Co., Ltd.. The 510(k) number is K203808.
When was Multi-unit Abutment, Multi-unit Angled Abutment approved by the FDA?
Multi-unit Abutment, Multi-unit Angled Abutment received FDA 510(k) clearance on 2021-10-20, under approval number K203808.
What company makes Multi-unit Abutment, Multi-unit Angled Abutment?
Multi-unit Abutment, Multi-unit Angled Abutment is manufactured by Megagen Implant Co., Ltd..
What is the FDA product code for Multi-unit Abutment, Multi-unit Angled Abutment?
The FDA product code for Multi-unit Abutment, Multi-unit Angled Abutment is NHA.
Related Clinical Trials
Other Devices by Megagen Implant 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.