LZW — Monitor, Spine Curvature Class U

FDA Device Classification

FDA product code LZW covers "Monitor, Spine Curvature", a Class U medical device. Submissions are reviewed by the Unknown panel. At least 5 recent 510(k) clearances have been granted under this product code.

Classification Details

Product Code
LZW
Device Class
Class U
Regulation Number
Submission Type
Review Panel
PM
Medical Specialty
Unknown
Implant
No

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K093553perseus altheticsPOSTURETEKAugust 13, 2010
K081540peter fischerZEGRA POSTURE TRAINERFebruary 20, 2009
K951244dan klineSPINE TUNER POSTURE TRAINERJune 26, 1995
K902669bagradBPA, BODY POSITION ALARMJuly 27, 1990
K884976mcdowell entMICRO-STRAIGHT POSTURE TRAINING DEVICEJune 9, 1989