# K990713: Spectranetics Lead Locking Device (LLD) #1, #2, #3 Lister

- Pathway: 510(k) (Traditional)
- Applicant: Spectranetics Corp.
- Decided: Oct 22, 1999 after 232 days
- Product code: DRB (Stylet, Catheter)
- Device class: 2
- Regulation: 21 CFR 870.1380
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 1 generation back to K970690 (1997). 1 ancestor in all.
1 later device descends 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)
- K970690: Locking Stylet 2, Cook Pacemaker Corp. (1997) Summary page 1.

## Most influential descendants
- K043401: Spectranetics LLD CS, Model 518-039 (2005), 0 descendants of its own

## Indications for use
The Spectranetics Lead Locking Devices, LLD™, are intended for use in patients suitable for transvernous removal of chronically iniplanted pacing or defibrillator leads having an inner lumen and using a superior venous approach. The lead inner lumen must have an inner diameter (ID) range from 0.013 — 0.032 inches (0.33 — 0.81 mm) and a length less than 25.6 inches (65 cm).

Source page: https://510kreport.com/device/K990713
Methodology: https://510kreport.com/methodology