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FDA 510(k)

Straumann Screw Retained Abutments

K-Number: K171757 · 2017-11-27

ApplicantStraumann USA, LLC (On Behalf of Institut Straumann Ag)
Decision Date2017-11-27
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

Straumann Screw Retained Abutments is a medical device manufactured by Straumann USA, LLC (On Behalf of Institut Straumann Ag). It received FDA 510(k) clearance on 2017-11-27 under approval number K171757. 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 Screw Retained Abutments?

Straumann Screw Retained Abutments is a medical device that received FDA 510(k) clearance on 2017-11-27. It is manufactured by Straumann USA, LLC (On Behalf of Institut Straumann Ag). The 510(k) number is K171757.

When was Straumann Screw Retained Abutments approved by the FDA?

Straumann Screw Retained Abutments received FDA 510(k) clearance on 2017-11-27, under approval number K171757.

What company makes Straumann Screw Retained Abutments?

Straumann Screw Retained Abutments is manufactured by Straumann USA, LLC (On Behalf of Institut Straumann Ag).

What is the FDA product code for Straumann Screw Retained Abutments?

The FDA product code for Straumann Screw Retained Abutments is NHA.

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Other Devices by Straumann USA, LLC (On Behalf of Institut Straumann Ag)

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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.

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