GENIE PEEK Knotless Anchor

GUDID 08800298539204

5.5mm PEEK anchor

OSTEONIC CO.,Ltd.

Tendon/ligament bone anchor, non-bioabsorbable

• Primary Device ID: 08800298539204
• NIH Device Record Key: 33ac9004-5b37-4c88-8bb3-918806d9ef26
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: GENIE PEEK Knotless Anchor
• Version Model Number: 550PPSP
• Company DUNS: 688999370
• Company Name: OSTEONIC CO.,Ltd.
• 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: false
• 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	08800298539204 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K243470

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: 2025-02-14
• Device Publish Date: 2025-02-06

On-Brand Devices [GENIE PEEK Knotless Anchor]

• 08800298539211: 6.5mm PEEK anchor
• 08800298539204: 5.5mm PEEK anchor
• 08800298539198: 4.75mm PEEK anchor
• 08800298539181: 3.75mm PEEK anchor