# K052757: Pheron Peripheral Percutaneous Transluminal Angioplasty (Pta) Catheter

- Pathway: 510(k) (Special)
- Applicant: Biotronik AG
- Decided: Oct 28, 2005 after 28 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
No predicates in its family tree.
8 later devices descend from it; 2 cite it directly.
0 of 9 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K072765: Passeo 18 (2007), 7 descendants of its own
- K082933: Passeo-35 Pta Catheter (2008), 5 descendants of its own
- K142379: Passeo-35 PTA Catheter (2014), 3 descendants of its own
- K222065: Passeo-35 Xeo Peripheral Dilatation Catheter (2023), 1 descendant of its own
- K151744: Passeo-18 Peripheral Dilation Catheter (2015), 1 descendant of its own

Source page: https://510kreport.com/device/K052757
Methodology: https://510kreport.com/methodology