CAVUX™ Cervical Cage-L 8x14x17mm PD-31-611

GUDID 10852776006352

CAVUX™ Cervical Cage-L implants are titanium constructs offered in various heights. All CAVUX™ Cervical Cage-L implants are manufactured from implant grade titanium alloy (6Al-4V ELI Titanium). The implants are provided sterile and are single-use only.

PROVIDENCE MEDICAL TECHNOLOGY, INC.

Implantable cervical facet joint distractor

• Primary Device ID: 10852776006352
• NIH Device Record Key: ff94fcd6-7dde-41b0-87bb-3ef6bc15d201
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: CAVUX™ Cervical Cage-L 8x14x17mm
• Version Model Number: PD-31-611
• Catalog Number: PD-31-611
• Company DUNS: 969820245
• Company Name: PROVIDENCE MEDICAL TECHNOLOGY, INC.
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Unsafe
• 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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00852776006355 [Primary]
GS1	10852776006352 [Package]; Contains: 00852776006355; Package: Box [1 Units]; In Commercial Distribution

FDA Product Code

• OVE: Intervertebral Fusion Device With Integrated Fixation, Cervical

Sterilization

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

[10852776006352]

Radiation Sterilization

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-06-22
• Device Publish Date: 2017-06-28

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