# K203740: JuggerKnot Soft Anchor

- Pathway: 510(k) (Traditional)
- Applicant: Riverpoint Medical
- Decided: Feb 12, 2021 after 52 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: 9 generations back to K792022 (1979). 60 ancestors in all.
5 later devices descend from it; 3 cite it directly.
0 of 66 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K150768: JuggerKnot Soft Anchors, Biomet Manufacturing Corp (2015) Summary page 4.

## Most influential descendants
- K232411: JuggerKnot Soft Anchor OC (2023), 2 descendants of its own
- K242494: OsseoFit Interfacing Anchor; OsseoFit Bone Tunnel Construct (2024), 0 descendants of its own
- K243203: OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor (2024), 0 descendants of its own
- K240719: OC JuggerKnot Soft Anchor (2024), 0 descendants of its own
- K231128: JuggerKnot Soft Anchor (2023), 0 descendants of its own

## Indications for use
Indicated for use in soft tissue to bone fixation for the following indications: Knee MPFL Knee Patellar tendon repair Knee MCL Knee Quadriceps tendon repair Hip Acetabular labral repair Hip Proximal hamstring repair. Hip Hip labral reconstruction. Foot and Ankle Achilles tendon repair Foot and Ankle Medial/lateral repair and reconstruction Foot and Ankle Plantar plate repair Foot and Ankle Mid- and forefoot repair Foot and Ankle Metatarsal ligament/tendon repair or reconstruction Shoulder Rotator Cuff Shoulder Shoulder Instability Shoulder Biceps Tenodesis Elbow Lateral epicondylitis repair Elbow Biceps tendon reattachment

Source page: https://510kreport.com/device/K203740
Methodology: https://510kreport.com/methodology