← Product Code [LOD](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LOD) · N18466

# CMW BONE CEMENT (N18466)

_Depuy, Inc. · LOD · Feb 22, 1984 · Orthopedic · APRL_

**Canonical URL:** https://fda.innolitics.com/submissions/ORTHOPEDIC/subpart-d%E2%80%94prosthetic-devices/LOD/N18466

## Device Facts

- **Applicant:** Depuy, Inc.
- **Product Code:** [LOD](/submissions/OR/subpart-d%E2%80%94prosthetic-devices/LOD.md)
- **Decision Date:** Feb 22, 1984
- **Decision:** APRL
- **Regulation:** 21 CFR 888.3027
- **Device Class:** Class 2
- **Review Panel:** Orthopedic

## Regulatory Identification

Polymethylmethacrylate (PMMA) bone cement is a device intended to be implanted that is made from methylmethacrylate, polymethylmethacrylate, esters of methacrylic acid, or copolymers containing polymethylmethacrylate and polystyrene. The device is intended for use in arthroplastic procedures of the hip, knee, and other joints for the fixation of polymer or metallic prosthetic implants to living bone.

## Special Controls

*Classification.* Class II (special controls). The special control for this device is the FDA guidance document entitled “Class II Special Controls Guidance Document: Polymethylmethacrylate (PMMA) Bone Cement.”

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**Source:** [https://fda.innolitics.com/submissions/ORTHOPEDIC/subpart-d%E2%80%94prosthetic-devices/LOD/N18466](https://fda.innolitics.com/submissions/ORTHOPEDIC/subpart-d%E2%80%94prosthetic-devices/LOD/N18466)

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