510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K923792Substantially Equivalent

Quantec Spinal Measuement System

Quantec Image Processing, Ltd., Madison NJ / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K923792 is the FDA 510(k) clearance record for QUANTEC SPINAL MEASUEMENT SYSTEM, cleared for Quantec Image Processing , Ltd. on under FDA product code LDK (Device, Sensing, Optical Contour). FDA records list one 510(k) clearance for Quantec Image Processing , Ltd. As of , FDA records show no recalls naming K923792.

Clearance record

Decision date
Received
(631 days to decision)
Product code
LDK Device, Sensing, Optical Contour
Device class
Unclassified
Review panel
Unknown
Applicant
Quantec Image Processing , Ltd. 37 King Rd., Madison NJ
510(k) summary
Statement
Third party review
No

Clearances, product code LDK

Trailing 12 months

FDA records hold no clearances under product code LDK in the trailing twelve months.

FDA records show no clearances under product code LDK in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LDK, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260