510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K890075Substantially Equivalent

Foottrak

Motion Analysis Corp., Santa Rosa CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K890075 is the FDA 510(k) clearance record for FOOTTRAK, a class II device, cleared for Motion Analysis Corp. on under FDA product code LXJ (Interactive Rehabilitation Exercise Devices). FDA records list 4 510(k) clearances for Motion Analysis Corp., from to . As of , FDA records show no recalls naming K890075.

Clearance record

Decision date
Received
(25 days to decision)
Product code
LXJ Interactive Rehabilitation Exercise Devices
Regulation
21 CFR 890.5360
Device class
Class II
Review panel
Physical Medicine
Applicant
Motion Analysis Corp. 3650 N. Laughlin Rd., Santa Rosa CA
Third party review
No

Clearances, product code LXJ

Trailing 12 months

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

FDA records show no clearances under product code LXJ in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code LXJ, 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