QES

Reherniation Reduction Device

Product code

QES

Device name

Reherniation Reduction Device

Device class

Class 3

Medical specialty

Unknown

Marketing pathway

PMA

Flag

Implant

FDA classification definition

The device is intended to reduce the incidence of reherniation, and reoperation following primary limited lumbar discectomy procedures (excision of herniated intervertebral disc).

Definition text from the FDA device classification database (U.S. federal government work, public domain).