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Modification to NuVasive Lateral Plate System

by Nuvasive, Inc.

510(k) K070273

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Special NumberK070273 Date3 Apr 2007ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
KWQ
Device class
Class II
Regulation
21 CFR Part 888.3060
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Related clearances

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Overview

AI-generated summary, 21 Sep 2026

Written by a language model from registry data. Not verified by deviCERTS or the manufacturer. The registry data above is the record.

The Modification to NuVasive Lateral Plate System consists of spinal implants including plates, screws, bolts, and locking nuts, providing rigid fixation of the spine. These implants are configured to address specific patient pathology and anatomical conditions and are implanted via lateral, anterolateral, or anterior surgical approaches.

The system provides mechanical stabilization of the spine and is used by surgeons during procedures. It is supplied as a modification to an existing system and is authorized under FDA 510K clearance with product code KWQ. The device is intended for use in orthopedic applications and is available in various sizes and configurations.

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