# K152934: MMS PTA Balloon Catheter

- Pathway: 510(k) (Traditional)
- Applicant: Micro Medical Solutions, Inc.
- Decided: Apr 25, 2016 after 203 days
- Product code: LIT (Catheter, Angioplasty, Peripheral, Transluminal)
- Device class: 2
- Regulation: 21 CFR 870.1250
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 2 generations back to K090822 (2009). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K122940: Advance Micro 14 Ultra Low Profile Balloon Dilatation Catheter Model PTA3, Cook, Inc. (2013) Summary page 4.

## Indications for use
The Micro Medical Solutions PTA Balloon Catheter is intended for percutaneous transluminal angioplasty (PTA) of lesions in peripheral arteries including anterior tibial, posterior tibial, and pedal. Not for use in coronary arteries.

Source page: https://510kreport.com/device/K152934
Methodology: https://510kreport.com/methodology