NXT

Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing

Product code
NXT
Device name
Prosthesis, Hip, Semi-Constrained, Metal/Metal, Resurfacing
Device class
Class 3
Medical specialty
Unknown
Marketing pathway
PMA
Flag
Implant

FDA classification definition

Prosthesis, hip, semi-constrained, metal/metal, resurfacing device relieves hip pain and improves hip function by replacing the parts of the hip that have been severely damaged by degenerative joint diseases. This device is indicated for patients with degenerative joint diseases including osteoarthritis, rheumatoid arthritis, traumatic arthritis, dysplasia, or avascular necrosis and for patients who, due to their relatively younger age or increased activity level, may not be suitable for traditional total hip replacement due to an increased possibility of requiring future hip joint revision.

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

Official FDA classification page: NXT
Classification and pathway per current FDA publications. Data from openFDA (CC0).