# K050227: Threvo Suture Anchor with Disposable Driver

- Pathway: 510(k) (Special)
- Applicant: Linvatec Corp.
- Decided: Mar 2, 2005 after 29 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: 1 generation back to K003984 (2001). 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)
- K003984: Super Revo Suture Anchor, Linvatec Corp. (2001) Summary page 2.

## Indications for use
The ThRevo Suture Anchor with Disposable Driver is intended to be used for rotator cuff repairs in the shoulder either arthroscopically or in a mini-open technique.

Source page: https://510kreport.com/device/K050227
Methodology: https://510kreport.com/methodology