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FDA 510(k)

ES2 Neuromonitoring Accessory Instruments

K-Number: K171807 · 2017-07-18

ApplicantStryker Corporation
Decision Date2017-07-18
Product CodePDQ
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

ES2 Neuromonitoring Accessory Instruments is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corporation. It received FDA 510(k) clearance on 2017-07-18 under 510(k) number K171807. The device is classified under product code PDQ. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ES2 Neuromonitoring Accessory Instruments?

ES2 Neuromonitoring Accessory Instruments is a medical device that received FDA 510(k) clearance on 2017-07-18. The listed applicant is Stryker Corporation. The 510(k) number is K171807.

When did ES2 Neuromonitoring Accessory Instruments receive FDA 510(k) clearance?

ES2 Neuromonitoring Accessory Instruments received FDA 510(k) clearance on 2017-07-18, under 510(k) number K171807.

Who is the listed applicant for ES2 Neuromonitoring Accessory Instruments?

The FDA 510(k) record lists Stryker Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ES2 Neuromonitoring Accessory Instruments?

The FDA product code for ES2 Neuromonitoring Accessory Instruments is PDQ.

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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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