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)

Straumann Immediate Temporary Abutments

K-Number: K201681 · 2021-03-18

Decision Date2021-03-18
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Straumann Immediate Temporary Abutments is a medical device manufactured by Institut Straumann AG. It received FDA 510(k) clearance on 2021-03-18 under approval number K201681. 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 Immediate Temporary Abutments?

Straumann Immediate Temporary Abutments is a medical device that received FDA 510(k) clearance on 2021-03-18. It is manufactured by Institut Straumann AG. The 510(k) number is K201681.

When was Straumann Immediate Temporary Abutments approved by the FDA?

Straumann Immediate Temporary Abutments received FDA 510(k) clearance on 2021-03-18, under approval number K201681.

What company makes Straumann Immediate Temporary Abutments?

Straumann Immediate Temporary Abutments is manufactured by Institut Straumann AG.

What is the FDA product code for Straumann Immediate Temporary Abutments?

The FDA product code for Straumann Immediate Temporary Abutments is NHA.

Related Clinical Trials

Other Devices by Institut Straumann AG

View all 56 devices →

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.