TLIF Curved-L, 32 x 13mm

GUDID M739PL3213

TLIF Curved-L, 32 x 13mm

CAPTIVA SPINE, INC.

Polymeric spinal interbody fusion cage

• Primary Device ID: M739PL3213
• NIH Device Record Key: 80e63bbb-8b58-43e5-9336-a0416844b6b7
• Commercial Distribution Discontinuation: 2017-08-11
• Commercial Distribution Status: Not in Commercial Distribution
• Brand Name: TLIF Curved-L, 32 x 13mm
• Version Model Number: PL3213
• 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	M739PL3213 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K092017

FDA Product Code

• MAX: Intervertebral Fusion Device With Bone Graft, Lumbar

Sterilization

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

[M739PL3213]

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: 2015-08-28

On-Brand Devices [TLIF Curved-L, 32 x 13mm]

• M739PL3213: TLIF Curved-L, 32 x 13mm