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FDA 510(k)

Spine Guidance Software, Stryker Q Guidance System

K-Number: K220593 · 2022-05-27

ApplicantStryker Leibinger GmbH & Co KG
Decision Date2022-05-27
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Spine Guidance Software, Stryker Q Guidance System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Leibinger GmbH & Co KG. It received FDA 510(k) clearance on 2022-05-27 under 510(k) 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. The listed applicant is Stryker Leibinger GmbH & Co KG. The 510(k) number is K220593.

When did Spine Guidance Software, Stryker Q Guidance System receive FDA 510(k) clearance?

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

Who is the listed applicant for Spine Guidance Software, Stryker Q Guidance System?

The FDA 510(k) record lists Stryker Leibinger GmbH & Co KG as the applicant. This does not by itself establish the device manufacturer.

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.

Other records listing Stryker Leibinger GmbH & Co KG as applicant

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Related Devices (Code: OLO)

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.

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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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