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 a medical device manufactured by Stryker Corp.. It received FDA 510(k) clearance on 2019-07-12 under approval 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. It is manufactured by Stryker Corp.. The 510(k) number is K191259.
When was Stryker CrossFlow Integrated Arthroscopy Pump approved by the FDA?
Stryker CrossFlow Integrated Arthroscopy Pump received FDA 510(k) clearance on 2019-07-12, under approval number K191259.
What company makes Stryker CrossFlow Integrated Arthroscopy Pump?
Stryker CrossFlow Integrated Arthroscopy Pump is manufactured by Stryker Corp..
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.