# K120824: 3.9MM Reelx STT Suture Anchor System

- Pathway: 510(k) (Traditional)
- Applicant: Stryker Corp.
- Decided: Jul 18, 2012 after 121 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: 5 generations back to K012125 (2001). 26 ancestors in all.
1 later device descends from it; 1 cites it directly.
0 of 28 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K090530: Spin-Loc Suture Anchor System FG-0302-01,FG-0305-01, Ross Creek Medical, Inc. (2009) Summary page 1.
- K051219: Pushlock, Arthrex, Inc. (2005) Summary page 1.
- K970896: Mitek 3.5 MM Panalok Wedge Absorbable Suture Anchor System, ETHICON, Inc. (1997) Summary page 1.

## Most influential descendants
- K180759: SECULOK™ Suture Anchor (2018), 0 descendants of its own

## Indications for use
The ReelX SIT Suture Anchor System is indicated for use in fixating suture or soft tissue fixation to bone in the shoulder, foot and ankle, knee, and elbow. The anchor is indicated for use in the following procedures: Shoulder: Rotator Cuff Repair Bankart Repair SLAP Lesion Repair Biceps Tenodesis Acromio-Clavicular Separation Repair Deltoid Repair Capsular Shift/Capsulolabral Reconstruction Knee: Medial Collateral Ligament Repair Lateral Collateral Ligament Repair Patellar Tendon Repair Posterior Oblique Ligament Repair Illiotibial Band Tenodesis Foot and Ankde: Lateral Stabilization Medial Stabilization Achilles Tendon Repair Hallux Valgus Reconstruction Midfoot Reconstruction Metatarsal Ligament Repair Elbow: Biceps Tendon Reattachiment The ReeiX STT Suture Anchor System is intended for single-use only.

Source page: https://510kreport.com/device/K120824
Methodology: https://510kreport.com/methodology