HipCheck— 510(k) K230045

Substantially Equivalent

Stryker Corp.

FDA 510(k) clearance K230045 for HipCheck, Substantially Equivalent on 2023-09-29. Applicant: Stryker Corp.. Device class: 2.

Clearance details

Applicant: Stryker Corp.
Product code: Code QIH
Device class: Class 2
Regulation: 21 CFR 892.2050
Advisory panel: Radiology
Date received: 2023-01-06
Decision date: 2023-09-29
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Jose, CA, US

Download summary PDF View on FDA.gov ↗

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More clearances from Stryker Corp.

K191259 — Stryker CrossFlow Integrated Arthroscopy Pump2019-07-12
K182359 — HipCheck2018-12-13
K143399 — Stryker Footed Attachments and Cutting Accessories2015-05-08
K143320 — Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments2015-04-23
K150449 — LITe Plate System2015-03-20

Data sourced from openFDA. This site is unofficial and independent of the FDA.