LDK — Device, Sensing, Optical Contour Class U

FDA Device Classification

Classification Details

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

Recent 510(k) Clearances

K-NumberApplicantDevice NameDate
K230463nsiteNSite Scoliosis Assessment AppNovember 15, 2023
K232023momentum healthMomentum SpineOctober 4, 2023
K183485cryos technologiesCryoVizion SystemAugust 28, 2019
K923792quantec image processingQUANTEC SPINAL MEASUEMENT SYSTEMApril 20, 1994
K860225far orthopedicsMETRICOMFebruary 11, 1986
K851133terran biomedical instrumentsTERRAN BIOMECHANICAL ANALYSIS SYSTEMJune 19, 1985
K844736oxford medilogISISMarch 21, 1985
K800591bio-tek instrumentsCONTOUROGRAPH M-500April 2, 1980