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FDA 510(k)

Preview Shoulder

K-Number: K240172 · 2024-04-04

ApplicantGenesis Software Innovations
Decision Date2024-04-04
Product CodeQIH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

Preview Shoulder is the device name listed in this FDA 510(k) record. The listed applicant is Genesis Software Innovations. It received FDA 510(k) clearance on 2024-04-04 under 510(k) number K240172. 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 Preview Shoulder?

Preview Shoulder is a medical device that received FDA 510(k) clearance on 2024-04-04. The listed applicant is Genesis Software Innovations. The 510(k) number is K240172.

When did Preview Shoulder receive FDA 510(k) clearance?

Preview Shoulder received FDA 510(k) clearance on 2024-04-04, under 510(k) number K240172.

Who is the listed applicant for Preview Shoulder?

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

What is the FDA product code for Preview Shoulder?

The FDA product code for Preview Shoulder is QIH.

Other records listing Genesis Software Innovations as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K210556Preview Shoulder

Related Devices (Code: QIH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K253794Prostate CoreLucida Medical, Ltd.K252571mdprostateMediaire GmbHK253902RealGUIDE3DIEMME SRLK253835AffinityHermes Medical Solutions ABK260980cmAngio® V2.0Curemetrix, Inc.K261210Cleerly PlaqueCleerly, Inc.

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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