Code of Federal Regulations (Last Updated: July 5, 2024) |
Title 21 - Food and Drugs |
Chapter I - Food and Drug Administration, Department of Health and Human Services |
SubChapter H - Medical Devices |
Part 876 - Gastroenterology-Urology Devices |
Subpart D - Prosthetic Devices |
§ 876.3630 - Penile rigidity implant.
Latest version.
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§ 876.3630 Penile rigidity implant.
(a) Identification. A penile rigidity implant is a device that consists of a pair of semi-rigid rods implanted in the corpora cavernosa of the penis to provide rigidity. It is intended to be used in men diagnosed as having erectile dysfunction.
(b) Classification. Class II. The special control for this device is the FDA guidance entitled “Guidance for the Content of Premarket Notifications for Penile Rigidity Implants.”
[65 FR 4882, Feb. 2, 2000]