# K982313: Horizon Titanium Clips, Horizon Tantalum Clips

- Pathway: 510(k) (Traditional)
- Applicant: Weck Closure Systems
- Decided: Aug 10, 1998 after 40 days
- Product code: FZP (Clip, Implantable)
- Device class: 2
- Regulation: 21 CFR 878.4300
- Recalls of this device: 1 (0 Class I)
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
15 later devices descend from it; 6 cite it directly.
0 of 16 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K200166: Mirus Ligating Clip, Mirus Ligating Clip Applier (2020), 7 descendants of its own
- K212127: Picocaremajesty (2022), 6 descendants of its own
- K233018: PICOSECOND Nd:YAG Laser System (2023), 2 descendants of its own
- K233007: Picosecond Nd:YAG Laser System; PICO LEGEND (2024), 1 descendant of its own
- K132658: Hemoclip Traditional Ligating Clips, Hemoclip Plus Ligating Clips, Horizon Ligting Clips (2013), 1 descendant of its own

## Recalls of this device
- Aug 8, 2013 · Class II · Z-2327-2016: The manufacturing and expiration dates are not printed on the blister pack label.

## Indications for use
Horizon ligating clips are indicated for procedures involving vessels or anatomic structures where ligating clips are the best choice. Select clip size, type and material based upon experience, judgement and needs.

Source page: https://510kreport.com/device/K982313
Methodology: https://510kreport.com/methodology