# K090530: Spin-Loc Suture Anchor System FG-0302-01,FG-0305-01

- Pathway: 510(k) (Traditional)
- Applicant: Ross Creek Medical, Inc.
- Decided: May 20, 2009 after 82 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: 4 generations back to K012125 (2001). 24 ancestors in all.
2 later devices descend from it; 1 cites it directly.
0 of 27 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K063479: Arthrex Pushlock, Arthrex, Inc. (2006) Summary page 1.
- K063478: Versalok Anchor with Free Strands of Orthocord Suture (210808), Ethibond Suture (210809), and Panacryl Suture (210810), Depuy Mitek, A Johnson & Johnson Company (2006) Summary page 1.
- K063778: Force Fiber Polyethylene Nonabsorbable Suture, Teleflex Medical (2007) Summary page 1.

## Most influential descendants
- K120824: 3.9MM Reelx STT Suture Anchor System (2012), 1 descendant of its own
- K180759: SECULOK™ Suture Anchor (2018), 0 descendants of its own

## Indications for use
The Ross Creek Spin-Loc Suture Anchor System is intended to be used for soft tissue fixation to bone in the shoulder, foot and ankle, knee, and elbow. The anchor is intended 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 Elbow Biceps Tendon Reattachment Foot and Ankle Lateral Stabilization Medial Stabilization Achilles Tendon Repair Hallux Valgus Reconstruction Midfoot Reconstruction Metatarsal Ligament Repair The Ross Creek Spin-Loc Suture Anchor System is intended for single-use only.

Source page: https://510kreport.com/device/K090530
Methodology: https://510kreport.com/methodology