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FDA 510(k)

V3 Segmental Plating System

K-Number: K182418 · 2018-11-29

ApplicantAtlas Spine, Inc.
Decision Date2018-11-29
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

V3 Segmental Plating System is a medical device manufactured by Atlas Spine, Inc.. It received FDA 510(k) clearance on 2018-11-29 under approval number K182418. 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 V3 Segmental Plating System?

V3 Segmental Plating System is a medical device that received FDA 510(k) clearance on 2018-11-29. It is manufactured by Atlas Spine, Inc.. The 510(k) number is K182418.

When was V3 Segmental Plating System approved by the FDA?

V3 Segmental Plating System received FDA 510(k) clearance on 2018-11-29, under approval number K182418.

What company makes V3 Segmental Plating System?

V3 Segmental Plating System is manufactured by Atlas Spine, Inc..

What is the FDA product code for V3 Segmental Plating System?

The FDA product code for V3 Segmental 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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