OC JuggerLoop™ Soft Anchor SP

GUDID 00840277405081

Soft Anchor

RIVERPOINT MEDICAL, LLC

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 00840277405081
• NIH Device Record Key: f2f21f3d-c567-4bcd-a794-c2fc2e1b68ab
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OC JuggerLoop™ Soft Anchor SP
• Version Model Number: 120003963
• Company DUNS: 964053560
• Company Name: RIVERPOINT MEDICAL, LLC
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Safe
• Human Cell/Tissue Product: false
• Device Kit: false
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840277405081 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243203

FDA Product Code

• MBI: Fastener, Fixation, Nondegradable, Soft Tissue

Sterilization

• Steralize Prior To Use: false
• Device Is Sterile: true

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-12-27
• Device Publish Date: 2024-12-19

Devices Manufactured by RIVERPOINT MEDICAL, LLC

• 00840277407955 - JuggerKnotless Soft Anchor: 2025-08-06 Soft Anchor
• 00840277409966 - HS Fiber: 2025-08-06 Suture
• 00840277409973 - HS Fiber: 2025-08-06 Suture
• 00840277410153 - Silk: 2025-08-06 Suture
• 10840277408386 - Polybond: 2025-06-26 Suture
• 10840277408393 - Polybond: 2025-06-26 Suture
• 10840277408409 - Polybond: 2025-06-26 Suture
• 10840277408416 - Polybond: 2025-06-26 Suture