510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K830784Substantially Equivalent

Walk N Roll

Meta-Morris, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K830784 is the FDA 510(k) clearance record for WALK N ROLL, a class I device, cleared for Meta-Morris on under FDA product code ITJ (Walker, Mechanical). FDA records list one 510(k) clearance for Meta-Morris. As of , FDA records show no recalls naming K830784.

Clearance record

Decision date
Received
(75 days to decision)
Product code
ITJ Walker, Mechanical
Regulation
21 CFR 890.3825
Device class
Class I
Review panel
Physical Medicine
Applicant
Meta-Morris 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ITJ

Trailing 12 months

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

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