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FDA 510(k)

corra™ cervical plating system

K-Number: K260570 · 2026-04-22

ApplicantCarlsmed, Inc.
Decision Date2026-04-22
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

corra™ cervical plating system is a medical device manufactured by Carlsmed, Inc.. It received FDA 510(k) clearance on 2026-04-22 under approval number K260570. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the corra™ cervical plating system?

corra™ cervical plating system is a medical device that received FDA 510(k) clearance on 2026-04-22. It is manufactured by Carlsmed, Inc.. The 510(k) number is K260570.

When was corra™ cervical plating system approved by the FDA?

corra™ cervical plating system received FDA 510(k) clearance on 2026-04-22, under approval number K260570.

What company makes corra™ cervical plating system?

corra™ cervical plating system is manufactured by Carlsmed, Inc..

What is the FDA product code for corra™ cervical plating system?

The FDA product code for corra™ cervical plating system is KWQ.

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Related Devices (Code: KWQ)

K160982Sphynx™Eden Spine, LLC K162638CETRA Anterior Cervical Plate SystemOrthofix, Inc. K162194MEDICREA INTERNATIONAL Anterior Cervical Locking Plate SystemMedicrea International SA K162211AccuFit Lateral Plate SystemPrecision Spine, Inc. K162250FortiBridge Anterior Cervical Plate SystemNanovis Spine, LLC K162664Pyrenees Cervical Plate SystemK2m, 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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