Browse hierarchy: [Orthopedic (OR)](/submissions/OR) → [Subpart E — Surgical Devices](/submissions/OR/subpart-e%E2%80%94surgical-devices) → [21 CFR 888.4520](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.4520) → QLR — Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices

# QLR · Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices

_Orthopedic · 21 CFR 888.4520 · Class 2_

**Canonical URL:** https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QLR

## Overview

- **Product Code:** QLR
- **Device Name:** Manual Instruments Designed For Use With Non-Fusion Spinous Process Spacer Devices
- **Regulation:** [21 CFR 888.4520](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.4520)
- **Device Class:** 2
- **Review Panel:** [Orthopedic](/submissions/OR)

## Identification

Orthopedic manual surgical instrumentation for use with non-fusion spinous process spacer devices are non-powered hand-held devices designed specifically for use with non-fusion spinous process spacer devices and interface with the associated implant for the purpose of inserting, positioning, or removing the implant. This type of device includes instruments specific to the geometry of the implant.

## Classification Rationale

Class II (special controls). The special controls for this device are:

## Special Controls

*Classification.* Class II (special controls). The special controls for this device are:(1) Technical specifications regarding geometry of the instruments must be specified and validated to demonstrate that the instruments can safely position, place, or remove the implant.
(2) The patient contacting components of the device must be demonstrated to be biocompatible.
(3) Performance data must demonstrate that reprocessing of reusable devices that are provided non-sterile, or sterilization of devices provided sterile, is validated.
(4) Labeling must include:
(i) Identification of implant(s) and instruments which have been validated for use together; and
(ii) Validated methods and instructions for reprocessing any reusable parts.

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K253118](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QLR/K253118.md) | Companion Spine DIAM™ Instrumentation | Companion Spine France | Dec 16, 2025 | SESE |

## Top Applicants

- Companion Spine France — 1 clearance

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**Source:** [https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QLR](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/QLR)

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