# K063025: Lina Powerblade, Model 5005,5005-E,5005-C,5005-150,5000-C-150,5005-E-C-150,5005-420,5005-C-420,5005-E-420,5005-E-C-420,

- Pathway: 510(k) (Traditional)
- Applicant: Lina Medical Aps
- Decided: Dec 1, 2006 after 60 days
- Product code: GEI (Electrosurgical, Cutting & Coagulation & Accessories)
- Device class: 2
- Regulation: 21 CFR 878.4400
- 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’s file for it is a 510(k) statement, which names no predicate.

## Most influential descendants
- K132837: Lina Powerblade Plus (2013), 1 descendant of its own
- K142757: LiNA PowerBlade Plus HC (2014), 0 descendants of its own

## Indications for use
The LiNA PowerBlade is intended for use in open and laparoscopic surgery where grasping, coagulating, and transecting is indicated.

Source page: https://510kreport.com/device/K063025
Methodology: https://510kreport.com/methodology