# K073481: Threvo Anchor, Disposable Driver, HI-FI Sutures

- Pathway: 510(k) (Special)
- Applicant: Conmed Linvatec
- Decided: Jan 7, 2008 after 27 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: 2 generations back to K003984 (2001). 2 ancestors in all.
57 later devices descend from it; 1 cites it directly.
0 of 60 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K041713: Super Revo Herculine Suture Anchor, Linvatec Corp. (2004) Summary page 1.

## Most influential descendants
- K091549: Conmed Linvatec Soft Tissue to Bone System (2009), 56 descendants of its own
- K111779: Y-Knot All-Suture Anchor Model HF13 (2011), 29 descendants of its own
- K131035: Y-Knot Flex All-Suture Anchor, W/ Two #2 (5 Metric) HI-FI Sutures, 1.8MM (2013), 17 descendants of its own
- K133224: Y-Knot RC All-Suture Anchor, 2.8MM - Double Loaded and Triple Loaded W/ #2 Hifi Sutures (2014), 12 descendants of its own
- K163258: CrossFT Knotless Suture Anchor with Disposable Driver (2017), 9 descendants of its own

## Indications for use
The ThRevo® Anchor, Disposable Driver, Hi-FiTM Sutures 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/K073481
Methodology: https://510kreport.com/methodology