Universal Base Abutment
K-Number: K180899 · 2018-10-31
ApplicantNobel Biocare AB
Decision Date2018-10-31
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Universal Base Abutment is a medical device manufactured by Nobel Biocare AB. It received FDA 510(k) clearance on 2018-10-31 under approval number K180899. 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 Universal Base Abutment?
Universal Base Abutment is a medical device that received FDA 510(k) clearance on 2018-10-31. It is manufactured by Nobel Biocare AB. The 510(k) number is K180899.
When was Universal Base Abutment approved by the FDA?
Universal Base Abutment received FDA 510(k) clearance on 2018-10-31, under approval number K180899.
What company makes Universal Base Abutment?
Universal Base Abutment is manufactured by Nobel Biocare AB.
What is the FDA product code for Universal Base Abutment?
The FDA product code for Universal Base Abutment is NHA.
Other Devices by Nobel Biocare AB
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K153015Transfer & Angled AbutmentOsstem Implant Co., Ltd.
K161435Temporary Snap AbutmentNobel Biocare AB
K160786RODO Abutment SystemRodo Medical, Inc.
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.