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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 a medical device manufactured by Genesis Software Innovations. It received FDA 510(k) clearance on 2024-04-04 under approval 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. It is manufactured by Genesis Software Innovations. The 510(k) number is K240172.

When was Preview Shoulder approved by the FDA?

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

What company makes Preview Shoulder?

Preview Shoulder is manufactured by Genesis Software Innovations.

What is the FDA product code for Preview Shoulder?

The FDA product code for Preview Shoulder is QIH.

Other Devices by Genesis Software Innovations

K210556Preview Shoulder

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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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