← Product Code [ETA](/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ETA) · K843461

# BIOGLASS OSSICULAR RECONSTRUCTION PROSTH (K843461)

_American Biomaterials Corp. · ETA · Jan 9, 1985 · Ear, Nose, Throat · SESE_

**Canonical URL:** https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ETA/K843461

## Device Facts

- **Applicant:** American Biomaterials Corp.
- **Product Code:** [ETA](/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ETA.md)
- **Decision Date:** Jan 9, 1985
- **Decision:** SESE
- **Submission Type:** Traditional
- **Regulation:** 21 CFR 874.3495
- **Device Class:** Class 2
- **Review Panel:** Ear, Nose, Throat

## Regulatory Identification

A total ossicular replacement prosthesis is a device intended to be implanted for the total functional reconstruction of the ossicular chain and facilitates the conduction of sound waves from the tympanic membrance to the inner ear. The device is made of materials such as polytetrafluoroethylene, polytetrafluoroethylene with vitreous carbon fibers composite, porous polyethylene, or from a combination of these materials.

---

**Source:** [https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ETA/K843461](https://fda.innolitics.com/submissions/EN/subpart-d%E2%80%94prosthetic-devices/ETA/K843461)

**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
