# K013063: Grip Lock Anchor, Model 411374

- Pathway: 510(k) (Traditional)
- Applicant: Medtronic Neurological
- Decided: Dec 11, 2001 after 90 days
- Product code: GZB (Stimulator, Spinal-Cord, Implanted (Pain Relief))
- Device class: 2
- Regulation: 21 CFR 882.5880
- 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 P970004 (1997). 2 ancestors in all.
No later device cites it as a predicate yet.
0 of 3 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K972906: Medtronic Twist Lock Anchor (Partnumber 103953/3550TLA), Medtronic Vascular (1998) Summary page 2.
- P970004: Medtronic Interstim Therapy System for Urinary Control, Medtronic Neuromodulation (1997) Summary page 3.

## Indications for use
The Medtronic Grip-lockm Anchor is indicated for use to facilitate Medtronic neurological lead fixation.

Source page: https://510kreport.com/device/K013063
Methodology: https://510kreport.com/methodology