QUANTEC SPINAL MEASUEMENT SYSTEM— 510(k) K923792

Name: FDA 510(k) clearance K923792
Creator: U.S. Food and Drug Administration
Published: 1994-04-20

Substantially Equivalent

Quantec Image Processing , Ltd.

FDA 510(k) clearance K923792 for QUANTEC SPINAL MEASUEMENT SYSTEM, Substantially Equivalent on 1994-04-20. Applicant: Quantec Image Processing , Ltd.. Device class: Unclassified.

Clearance details

Applicant: Quantec Image Processing , Ltd.
Product code: Code LDK
Device class: Unclassified
Advisory panel: Unknown
Date received: 1992-07-28
Decision date: 1994-04-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Madison, NJ, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LDK

view all

K230463 — NSite Scoliosis Assessment App2023-11-15
K232023 — Momentum Spine2023-10-04
K183485 — CryoVizion System2019-08-28
K860225 — METRICOM1986-02-11
K851133 — TERRAN BIOMECHANICAL ANALYSIS SYSTEM1985-06-19

Data sourced from openFDA. This site is unofficial and independent of the FDA.