Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue Technology
K-Number: K170456 · 2017-04-05
Device Summary
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.