# K003984: Super Revo Suture Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Linvatec Corp.
- Decided: Mar 19, 2001 after 83 days
- Product code: MAI (Fastener, Fixation, Biodegradable, Soft Tissue)
- Device class: 2
- Regulation: 21 CFR 888.3030
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
86 later devices descend from it; 2 cite it directly.
0 of 87 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. FDA has not posted a summary or statement for it, so its predicates are not known.

## Most influential descendants
- K041713: Super Revo Herculine Suture Anchor (2004), 84 descendants of its own
- K073481: Threvo Anchor, Disposable Driver, HI-FI Sutures (2008), 57 descendants of its own
- 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
- K061294: KFX Knotless Fixation System (2006), 19 descendants of its own

Source page: https://510kreport.com/device/K003984
Methodology: https://510kreport.com/methodology