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FDA 510(k)

HipCheck

K-Number: K230045 · 2023-09-29

ApplicantStryker Corp.
Decision Date2023-09-29
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HipCheck is a medical device manufactured by Stryker Corp.. It received FDA 510(k) clearance on 2023-09-29 under approval number K230045. The device is classified under product code QIH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HipCheck?

HipCheck is a medical device that received FDA 510(k) clearance on 2023-09-29. It is manufactured by Stryker Corp.. The 510(k) number is K230045.

When was HipCheck approved by the FDA?

HipCheck received FDA 510(k) clearance on 2023-09-29, under approval number K230045.

What company makes HipCheck?

HipCheck is manufactured by Stryker Corp..

What is the FDA product code for HipCheck?

The FDA product code for HipCheck is QIH.

Other Devices by Stryker Corp.

K182359HipCheck K191259Stryker CrossFlow Integrated Arthroscopy Pump PMA P050044Absorbable collagen hemostatic agent with thrombin

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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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