510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K030714Substantially Equivalent

Peak Motus

Peak Performance Technologies, Inc., Centinnial CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K030714 is the FDA 510(k) clearance record for PEAK MOTUS, a class II device, cleared for Peak Performance Technologies, Inc. on under FDA product code LXJ (Interactive Rehabilitation Exercise Devices). FDA records list one 510(k) clearance for Peak Performance Technologies, Inc. As of , FDA records show no recalls naming K030714.

Clearance record

Decision date
Received
(71 days to decision)
Product code
LXJ Interactive Rehabilitation Exercise Devices
Regulation
21 CFR 890.5360
Device class
Class II
Review panel
Physical Medicine
Applicant
Peak Performance Technologies, Inc. 7388 S. Revere Pky 901, Centinnial CO
510(k) summary
Summary PDF
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