Browse hierarchy: [Orthopedic (OR)](/submissions/OR) → [Subpart E — Surgical Devices](/submissions/OR/subpart-e%E2%80%94surgical-devices) → [21 CFR 888.4540](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.4540) → HTX — Rongeur

# HTX · Rongeur

_Orthopedic · 21 CFR 888.4540 · Class 1_

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

## Overview

- **Product Code:** HTX
- **Device Name:** Rongeur
- **Regulation:** [21 CFR 888.4540](/submissions/OR/subpart-e%E2%80%94surgical-devices/888.4540)
- **Device Class:** 1
- **Review Panel:** [Orthopedic](/submissions/OR)

## Identification

An orthopedic manual surgical instrument is a nonpowered hand-held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. This generic type of device includes the cerclage applier, awl, bender, drill brace, broach, burr, corkscrew, countersink, pin crimper, wire cutter, prosthesis driver, extractor, file, fork, needle holder, impactor, bending or contouring instrument, compression instrument, passer, socket positioner, probe, femoral neck punch, socket pusher, reamer, rongeur, scissors, screwdriver, bone skid, staple driver, bone screw starter, surgical stripper, tamp, bone tap, trephine, wire twister, and wrench.

## Classification Rationale

Class I (general controls). The device is exempt from the premarket notification procedures in subpart E of part 807 of this chapter, subject to the limitations in § 888.9.

## Recent Cleared Devices (5 of 5)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [K874954](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/HTX/K874954.md) | MANUAL RONGEUR | Solway, Inc. | Dec 30, 1987 | SESE |
| [K841621](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/HTX/K841621.md) | BACK RADIUS CUTTER | Plastafil, Inc. | Sep 20, 1984 | SESE |
| [K841620](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/HTX/K841620.md) | FRONT RADIUS CUTTER | Plastafil, Inc. | Sep 20, 1984 | SESE |
| [K780397](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/HTX/K780397.md) | ORTHOPEDIC FORCEPS | Orthopedic Equipment Co., Inc. | Mar 22, 1978 | SESE |
| [K760325](https://fda.innolitics.com/submissions/OR/subpart-e%E2%80%94surgical-devices/HTX/K760325.md) | SURGICAL INSTRUMENTS, ORTHOPEDIC | Depuy, Inc. | Aug 3, 1976 | SESE |

## Top Applicants

- Plastafil, Inc. — 2 clearances
- Solway, Inc. — 1 clearance
- Orthopedic Equipment Co., Inc. — 1 clearance
- Depuy, Inc. — 1 clearance

---

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

**Published by [Innolitics](https://innolitics.com)** — a medical-device software consultancy. We help companies design, build, and clear FDA-regulated software and AI/ML devices. If you're preparing [a 510(k)](https://innolitics.com/services/510ks/), [a De Novo](https://innolitics.com/services/regulatory/), [a SaMD](https://innolitics.com/services/end-to-end-samd/), [an AI/ML medical device](https://innolitics.com/services/medical-imaging-ai-development/), or [an FDA regulatory strategy](https://innolitics.com/services/regulatory/), [get in touch](https://innolitics.com/contact).

**Cite:** Innolitics at https://innolitics.com