510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K073521Substantially Equivalent

Musmate Walking Aid

Musmate, Ltd., Bath, Somerset, GB / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073521 is the FDA 510(k) clearance record for MUSMATE WALKING AID, a class I device, cleared for Musmate, Ltd. on under FDA product code OHI (Orthosis, Foot Drop). FDA's definition for product code OHI reads: "Aid for drop foot or similar disorders which have a lack of ankle dorsiflexion. Indicated for foot raising paresis". FDA records list one 510(k) clearance for Musmate, Ltd. As of , FDA records show no recalls naming K073521.

Clearance record

Decision date
Received
(52 days to decision)
Product code
OHI Orthosis, Foot Drop
Regulation
21 CFR 890.3475
Device class
Class I
Review panel
Physical Medicine
Applicant
Musmate, Ltd. 4 Ford Rd., Bath, Somerset, GB
510(k) summary
Summary PDF
Third party review
No

Clearances, product code OHI

Trailing 12 months

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

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