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 a medical device manufactured by Stryker Corporation. It received FDA 510(k) clearance on 2017-07-18 under approval 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. It is manufactured by Stryker Corporation. The 510(k) number is K171807.
When was ES2 Neuromonitoring Accessory Instruments approved by the FDA?
ES2 Neuromonitoring Accessory Instruments received FDA 510(k) clearance on 2017-07-18, under approval number K171807.
What company makes ES2 Neuromonitoring Accessory Instruments?
ES2 Neuromonitoring Accessory Instruments is manufactured by Stryker Corporation.
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.