# K142653: G-Lok and G-Lok XL Extender

- Pathway: 510(k) (Special)
- Applicant: T.A.G. Medical Products Corporation, Ltd.
- Decided: Oct 16, 2014 after 28 days
- Product code: MBI (Fastener, Fixation, Nondegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3040
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
Longest line of descent: 10 generations back to K792022 (1979). 57 ancestors in all.
No later device cites it as a predicate yet.
0 of 58 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K101616: The Grapplr and Grapplr Extender, Tag Medical Corp. (2011) Summary page 4.

## Indications for use
The G-Lok® and G-Lok® XL Extender are intended to provide suspension fixation for soft tissue to bone in the repair of the natural ligament or tendon disruption or assist in reconstruction surgeries and to assist in the management of reconstructive surgeries.

Source page: https://510kreport.com/device/K142653
Methodology: https://510kreport.com/methodology