Atlas FDA

MUSMATE WALKING AID

FDA 510(k) clearance K073521 · decided 2008-02-04

Clearance details

K-number
K073521
Device name
MUSMATE WALKING AID
Applicant
Musmate, Ltd.
Decision
Substantially Equivalent
Date received
2007-12-14
Decision date
2008-02-04
Days to decision
52 days
Clearance type
Traditional
Product code
OHI
Device class
1
Regulation number
890.3475
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Bath, Somerset, GB
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Musmate

The Builder collects up to 8 candidate devices side by side with yours, then exports the substantial-equivalence comparison scaffold. How it works

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Recalls involving this device

No recalls on record reference this clearance.