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Affix Spinous Process Plate System

by Nuvasive, Inc.

510(k) K131238

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

Registry data, not yet checked by deviCERTS. Source FDA 510(k), synced 22 Oct 2026. What this means

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK131238 Date2 Jul 2013ClearedStatusActive

Recalls

0 recalls · FDA

No FDA recalls found in the data synced 22 Oct 2026.

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  • Withdrawn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
PEK
Device class
Class II
Regulation
21 CFR Part 888.3050
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Overview

AI-generated summary, 22 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 Affix Spinous Process Plate System is a posterior, non-pedicle supplemental fixation device. It is designed for plate fixation and attachment to the spinous process to achieve supplemental fusion in the non-cervical spine, specifically from T1 to S1.

This device is indicated for use in conditions including degenerative disc disease, spondylolisthesis, and trauma such as fractures or dislocations. It has received FDA 510(k) clearance for clinical use.

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