Straumann Variobase Abutments
K-Number: K170354 · 2017-06-07
ApplicantInstitut Straumann AG
Decision Date2017-06-07
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent
Device Summary
Straumann Variobase Abutments is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2017-06-07 under approval number K170354. 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 Straumann Variobase Abutments?
Straumann Variobase Abutments is a medical device that received FDA 510(k) clearance on 2017-06-07. It is manufactured by Institut Straumann AG. The 510(k) number is K170354.
When was Straumann Variobase Abutments approved by the FDA?
Straumann Variobase Abutments received FDA 510(k) clearance on 2017-06-07, under approval number K170354.
What company makes Straumann Variobase Abutments?
Straumann Variobase Abutments is manufactured by Institut Straumann AG.
What is the FDA product code for Straumann Variobase Abutments?
The FDA product code for Straumann Variobase Abutments is NHA.
Related Clinical Trials
Other Devices by Institut Straumann AG
Related Devices (Code: NHA)
K161713Dentium CAD/CAM AbutmentsDentium Co., Ltd.
K160798IPS e.max® Press Abutment Solutions for Viteo Base TiIvoclar Vivadent, AG
K162004PREMIUM Implant Systems SHELTA Implant SystemsSweden & Martina S.P.A.
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.