# MFA · Device, Removal, Pacemaker Electrode, Percutaneous

_ ·  · Class 3_

**Canonical URL:** https://fda.innolitics.com/submissions/CV/CV-misc/MFA

## Overview

- **Product Code:** MFA
- **Device Name:** Device, Removal, Pacemaker Electrode, Percutaneous
- **Regulation:** 21 CFR N/A
- **Device Class:** 3
- **Review Panel:** [](/submissions/)

## Recent Cleared Devices (1 of 1)

| Record | Device Name | Applicant | Decision Date | Decision |
| --- | --- | --- | --- | --- |
| [P960042](https://fda.innolitics.com/submissions/CV/CV-misc/MFA/P960042.md) | SPECTRANETICS CVX-300 EXCIMER LASER SYSTEM & LASER SHEATH | Spectranetics (Philips) | Dec 9, 1997 | APPR |

## Top Applicants

- Spectranetics (Philips) — 1 clearance

---

**Source:** [https://fda.innolitics.com/submissions/CV/CV-misc/MFA](https://fda.innolitics.com/submissions/CV/CV-misc/MFA)

**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