Hollywood 93-4210

GUDID 10889981030988

Hollywood Modular Trial, 11mm x 30mm x 10mm

SEASPINE ORTHOPEDICS CORPORATION

Spinal implant trial

• Primary Device ID: 10889981030988
• NIH Device Record Key: 41bb5bb9-8041-4e0e-a507-a6a3c0d38bf0
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Hollywood
• Version Model Number: 93-4210
• Catalog Number: 93-4210
• Company DUNS: 079840876
• Company Name: SEASPINE ORTHOPEDICS CORPORATION
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: false
• Expiration Date: false
• 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: +1(760)727-8399
• Email: custsvcspine@seaspine.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	10889981030988 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082310

FDA Product Code

• MQP: Spinal vertebral body replacement device

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-01
• Device Publish Date: 2019-10-24

On-Brand Devices [Hollywood]

• 10889981180591: Hollywood Instrument Tray Level Top
• 10889981180584: Hollywood Instrument Tray Level Bottom
• 10889981180577: Hollywood Instrument Tray Case
• 10889981180560: Hollywood Instrument Tray Lid
• 10889981031022: Hollywood Modular Trial, 11mm x 30mm x 14mm
• 10889981031008: Hollywood Modular Trial, 11mm x 30mm x 12mm
• 10889981030988: Hollywood Modular Trial, 11mm x 30mm x 10mm