Curved Rod, 5.5 x 150 mm

GUDID M739245521500

Curved Rod, 5.5 x 150 mm Straight Rod, 5.5 x 130 mm

CAPTIVA SPINE, INC.

Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: M739245521500
• NIH Device Record Key: c5870435-1d11-49d2-9dc5-99b79a6d8c80
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Curved Rod, 5.5 x 150 mm
• Version Model Number: 2455-2150
• 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	M739245521500 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K120292

FDA Product Code

• MNH: Orthosis, Spondylolisthesis Spinal Fixation

Sterilization

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

[M739245521500]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-04-08
• Device Publish Date: 2019-03-29

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