Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR, NMPA) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Abutment for Bridges

K-Number: K153779 · 2016-03-31

ApplicantAltatec GmbH
Decision Date2016-03-31
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Abutment for Bridges is a medical device manufactured by Altatec GmbH. It received FDA 510(k) clearance on 2016-03-31 under approval number K153779. 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 Abutment for Bridges?

Abutment for Bridges is a medical device that received FDA 510(k) clearance on 2016-03-31. It is manufactured by Altatec GmbH. The 510(k) number is K153779.

When was Abutment for Bridges approved by the FDA?

Abutment for Bridges received FDA 510(k) clearance on 2016-03-31, under approval number K153779.

What company makes Abutment for Bridges?

Abutment for Bridges is manufactured by Altatec GmbH.

What is the FDA product code for Abutment for Bridges?

The FDA product code for Abutment for Bridges is NHA.

Other Devices by Altatec GmbH

Related Devices (Code: NHA)

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.