Class Class II

Spine Guidance 5.3 Software; Q Interbody Instruments; Elite Q Attachments; Elite Cutting Accessories (K252871)

K252871 2026-02-06 Traditional
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Description

Spine Guidance 5.3 Software; Q Interbody Instruments; Elite Q Attachments; Elite Cutting Accessories by Stryker Leibinger GmbH & Co KG, an FDA 510(k) cleared neurology device.

Regulatory Information

Device ClassClass Class II
510(k) NumberK252871
Clearance Date2026-02-06
Clearance TypeTraditional
Product CodeOLO
Regulation Number882.4560

Categories

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Predicate lineage for K252871

A 510(k) clearance is granted by showing substantial equivalence to an earlier legally marketed device, called the predicate. This lineage is named in the 510(k) summary document and is not published by the FDA as a connected dataset. Spine Guidance 5.3 Software; Q Interbody Instruments; Elite Q Attachments; Elite Cutting Accessories (K252871) cites 0 predicate devices and is itself cited by 1 later device.

Later devices that cite this one as their predicate

Devices that cite K252871
K numberDeviceApplicantYear
K253623Spine Guidance 5.4 Software; Spine Guidance 5.4 Upgrade; Sp...Stryker Leibinger GmbH & Co KG2026

Trace the full predicate network for K252871

A link appears here only where the predicate could be read from a published 510(k) summary. Where no summary exists or a reference cannot be resolved to a K number, no link is drawn, so a gap means unknown rather than none.

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