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FDA 510(k)

Stryker CrossFlow Integrated Arthroscopy Pump

K-Number: K191259 · 2019-07-12

ApplicantStryker Corp.
Decision Date2019-07-12
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Stryker CrossFlow Integrated Arthroscopy Pump is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2019-07-12 under 510(k) number K191259. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker CrossFlow Integrated Arthroscopy Pump?

Stryker CrossFlow Integrated Arthroscopy Pump is a medical device that received FDA 510(k) clearance on 2019-07-12. The listed applicant is Stryker Corp.. The 510(k) number is K191259.

When did Stryker CrossFlow Integrated Arthroscopy Pump receive FDA 510(k) clearance?

Stryker CrossFlow Integrated Arthroscopy Pump received FDA 510(k) clearance on 2019-07-12, under 510(k) number K191259.

Who is the listed applicant for Stryker CrossFlow Integrated Arthroscopy Pump?

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

What is the FDA product code for Stryker CrossFlow Integrated Arthroscopy Pump?

The FDA product code for Stryker CrossFlow Integrated Arthroscopy Pump is HRX.

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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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