Lordotic Cage, 12 x 13mm

GUDID M739FCL12130

Lordotic Cage, 12 x 13mm

CAPTIVA SPINE, INC.

Polymeric spinal interbody fusion cage

• Primary Device ID: M739FCL12130
• NIH Device Record Key: bdd50576-51bb-4dea-8209-45700c814aa1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Lordotic Cage, 12 x 13mm
• Version Model Number: FCL1213
• Company DUNS: 836975784
• Company Name: CAPTIVA SPINE, 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: 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

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	M739FCL12130 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K110585

FDA Product Code

• ODP: Intervertebral Fusion Device With Bone Graft, Cervical

Sterilization

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

[M739FCL12130]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2020-02-24
• Device Publish Date: 2015-10-23

Devices Manufactured by CAPTIVA SPINE, INC.

• 00850065741567 - Trial 7mm: 2025-08-27 7mm Trial
• 00850065741574 - Trial 8mm: 2025-08-27 8mm Trial
• 00850065741581 - Trial 9mm: 2025-08-27 9mm Trial
• 00850065741598 - Trial 10mm: 2025-08-27 10mm Trial
• 00850065741604 - Trial 11mm: 2025-08-27 11mm Trial
• 00850065741611 - Trial 12mm: 2025-08-27 12mm Trial
• 00850065741628 - Distraction Paddle - 7mm: 2025-08-27 Distraction Paddle - 7mm
• 00850065741635 - Distraction Paddle - 8mm: 2025-08-27 Distraction Paddle - 8mm