# K140272: Swift-Lock Anchor

- Pathway: 510(k) (Traditional)
- Applicant: St Jude Medical
- Decided: May 2, 2014 after 88 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 K092371 (2009). 1 ancestor in all.
No later device cites it as a predicate yet.
0 of 2 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K092371: Swift-Lock Anchor, Model 1192, Advanced Neuromodulation Systems (2009) Summary page 1.

## Indications for use
SJM Neurostimulation Systems are indicated for spinal cord stimulation (SCS) in the management of chronic pain of the trunk and limbs, either as the sole mitigating agent, or as an adjunct to other modes of therapy used in a multidisciplinary approach. The Swift-Lock Anchor is intended to be an accessory to the leads component of the spinal cord stimulation (SCS) system, functioning to secure compatible St. Jude Medical (SJM) leads to the fascia or interspinous/supraspinous ligament.

Source page: https://510kreport.com/device/K140272
Methodology: https://510kreport.com/methodology