# K243203: OC JuggerKnotless Soft Anchor; OC JuggerLoop Soft Anchor

- Pathway: 510(k) (Special)
- Applicant: Riverpoint Medical
- Decided: Oct 29, 2024 after 28 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: 11 generations back to K792022 (1979). 62 ancestors in all.
No later device cites it as a predicate yet.
0 of 63 devices in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- K232411: JuggerKnot Soft Anchor OC, Riverpoint Medical, LLC (2023) Summary page 5.

## Indications for use
The OC JuggerKnotless Soft Anchor and OC JuggerLoop Soft Anchor are intended for use in soft tissue to bone fixation in the following indications: Knee MPFL Knee Patellar tendon repair Knee MCL Knee Quadriceps tendon repair 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/K243203
Methodology: https://510kreport.com/methodology