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FDA 510(k)

Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology

K-Number: K170456 · 2017-04-05

Decision Date2017-04-05
Product CodeNLQ
DecisionSubstantially Equivalent

Device Summary

Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology is a medical device manufactured by Stryker Sustainability Solutions. It received FDA 510(k) clearance on 2017-04-05 under approval number K170456. The device is classified under product code NLQ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology?

Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology is a medical device that received FDA 510(k) clearance on 2017-04-05. It is manufactured by Stryker Sustainability Solutions. The 510(k) number is K170456.

When was Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology approved by the FDA?

Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology received FDA 510(k) clearance on 2017-04-05, under approval number K170456.

What company makes Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology?

Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology is manufactured by Stryker Sustainability Solutions.

What is the FDA product code for Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology?

The FDA product code for Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology is NLQ.

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Official Source

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