# K000763: PX 53/15-BP, Model 130 050 and PX 60/15-BP, Model 130 051

- Pathway: 510(k) (Special)
- Applicant: Biotronik, GmbH & Co.
- Decided: Apr 6, 2000 after 28 days
- Product code: DTB (Permanent Pacemaker Electrode)
- Device class: 3
- Regulation: 21 CFR 870.3680
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
2 later devices descend from it; 1 cites it directly.
0 of 3 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
- K021217: Arox 53-BP; Arox 60-BP; Arox 45-JBP; Arox 53-JBP (2002), 1 descendant of its own
- K023099: Arox 45-JBP; Arox 53-JBP; Merox 45-JBP; Merox 53-JBP (2002), 0 descendants of its own

Source page: https://510kreport.com/device/K000763
Methodology: https://510kreport.com/methodology