# K060714: HI-FI Ultrafix Knotless Minimite Suture Anchor

- Pathway: 510(k) (Special)
- Applicant: Conmed Linvatec
- Decided: Apr 6, 2006 after 20 days
- Product code: HWC (Screw, Fixation, Bone)
- 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 K022827 (2002). 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)
- K022827: Ultrafix Knotless Minimite Suture Anchor, Linvatec Corp. (2002) Summary page 1.

## Indications for use
The Conmed Linvatec Hi-FiTM UltraFix® Knotless Minimite® Suture Anchor is intended for reattaching soft tissue to glenoid bone in the shoulder. The following are the indications for use: Bankart lesions, SLAP lesions, capsular shifts, capsulolabral reconstructions.

Source page: https://510kreport.com/device/K060714
Methodology: https://510kreport.com/methodology