FDA 510(k)

Spine Guidance Software, Stryker Q Guidance System

K-Number: K220593 · 2022-05-27

Decision Date2022-05-27

Product CodeOLO

Advisory CommitteeNE

DecisionSubstantially Equivalent

Device Summary

Spine Guidance Software, Stryker Q Guidance System is a medical device manufactured by Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2022-05-27 under approval number K220593. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Spine Guidance Software, Stryker Q Guidance System?

Spine Guidance Software, Stryker Q Guidance System is a medical device that received FDA 510(k) clearance on 2022-05-27. It is manufactured by Stryker Leibinger GmbH & Co KG. The 510(k) number is K220593.

When was Spine Guidance Software, Stryker Q Guidance System approved by the FDA?

Spine Guidance Software, Stryker Q Guidance System received FDA 510(k) clearance on 2022-05-27, under approval number K220593.

What company makes Spine Guidance Software, Stryker Q Guidance System?

Spine Guidance Software, Stryker Q Guidance System is manufactured by Stryker Leibinger GmbH & Co KG.

What is the FDA product code for Spine Guidance Software, Stryker Q Guidance System?

The FDA product code for Spine Guidance Software, Stryker Q Guidance System is OLO.

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Related Devices (Code: OLO)

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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.