FDA Product Code KWT: Prosthesis, Shoulder, Non-constrained, Metal/polymer Cemented
Under FDA product code KWT, non-constrained shoulder prostheses with metal and polymer bearing surfaces are cleared for shoulder hemiarthroplasty and total arthroplasty.
Non-constrained designs rely on intact rotator cuff function and soft tissue balance for joint stability rather than mechanical constraint. They are indicated in patients with preserved rotator cuff integrity and normal glenoid bone stock.
KWT devices are Class II medical devices, regulated under 21 CFR 888.3650 and reviewed by the FDA Orthopedic panel.
Leading manufacturers include Biomet, Inc., Zimmer, Inc. and Intermedics Orthopedics.
71
Total
71
Cleared
131d
Avg days
1979
Since
71 devices
Cleared
Mar 26, 1991
GLOBAL TOTAL SHOULDER
Depuy, Inc.
Orthopedic
89d
Cleared
Oct 15, 1987
NEER-III GLENOID RESURFACING PROSTHESIS
Kirschner Medical Corp.
Orthopedic
69d
Cleared
Oct 15, 1987
NEER-III OSTEOARTHRITIS GLENOID RESURFACE PROSTHE.
Kirschner Medical Corp.
Orthopedic
37d
Cleared
Oct 15, 1987
NEER-III SOLID KEEL GLENOID RESURFACING PROSTHESIS
Kirschner Medical Corp.
Orthopedic
37d
Cleared
Aug 27, 1987
BIOMET MODULAR SHOULDER PROSTHESIS
Biomet, Inc.
Orthopedic
65d
Cleared
Nov 07, 1983
MONOSPHERICAL RESURFACING GLENOID PROS
Howmedica Corp.
Orthopedic
38d
Cleared
Jun 03, 1983
GLENOID RESURFACING COMPONENT-3M-10816
3M Company
Orthopedic
49d
Cleared
Jun 02, 1983
GLENOID RESURFACE COMPONENT PMN 3M
3M Company
Orthopedic
48d
Cleared
Dec 01, 1980
GRISTINA GLENOID PROSTHESIS
Howmedica Corp.
Orthopedic
88d
Cleared
Jun 22, 1979
ZIMMER R TOTAL SHOULDER II
Zimmer, Inc.
Orthopedic
28d