AlternatiV+ Screw-In Anchor 20BN5503

GUDID 00850005827375

5.5MM SCREW-IN SUTURE ANCHOR

Genesis Biologics, Inc.

Tendon/ligament bone anchor, bioabsorbable

• Primary Device ID: 00850005827375
• NIH Device Record Key: 27975b0e-8aec-4129-ba67-ec471a6ae17e
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AlternatiV+ Screw-In Anchor
• Version Model Number: 20BN5503
• Catalog Number: 20BN5503
• Company DUNS: 016463487
• Company Name: Genesis Biologics, Inc.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: Labeling does not contain MRI Safety Information
• 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: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM
• Phone: 657-888-6243
• Email: ORDERS@GENESISBIOLOGICS.COM

Device Dimensions

• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter
• Outer Diameter: 5.5 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850005827375 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K230892

FDA Product Code

• MAI: Fastener, Fixation, Biodegradable, 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: 2024-10-16
• Device Publish Date: 2024-10-08

On-Brand Devices [AlternatiV+ Screw-In Anchor]

• 00850005827375: 5.5MM SCREW-IN SUTURE ANCHOR
• 00850005827368: 4.75MM SCREW-IN SUTURE ANCHOR