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FDA 510(k)

HipCheck

K-Number: K182359 · 2018-12-13

ApplicantStryker Corp.
Decision Date2018-12-13
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

HipCheck is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2018-12-13 under 510(k) number K182359. The device is classified under product code LLZ. 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 2018-12-13. The listed applicant is Stryker Corp.. The 510(k) number is K182359.

When did HipCheck receive FDA 510(k) clearance?

HipCheck received FDA 510(k) clearance on 2018-12-13, under 510(k) number K182359.

Who is the listed applicant for HipCheck?

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 HipCheck?

The FDA product code for HipCheck is LLZ.

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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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