ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT A004.7250

GUDID B922A00472500

ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT

INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED

Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: B922A00472500
• NIH Device Record Key: 84c752d3-3f25-45ff-abb2-fecc2fd06455
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT
• Version Model Number: A004.7250
• Catalog Number: A004.7250
• Company DUNS: 860396609
• Company Name: INDIUS MEDICAL TECHNOLOGIES PRIVATE LIMITED
• 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

Customer Support Contacts

• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com
• Phone: +1(214)972-8683
• Email: info@indiusmedical.com

Device Dimensions

• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter
• Outer Diameter: 5.5 Millimeter
• Length: 50 Millimeter

Device Identifiers

Device Issuing Agency	Device ID
HIBCC	B922A00472500 [Primary]

FDA Product Code

• NKB: Thoracolumbosacral Pedicle Screw System

Sterilization

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

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

[B922A00472500]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2022-10-20
• Device Publish Date: 2022-10-12

On-Brand Devices [ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT]

• B922A00472500: ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT
• B922A00572500: ACURA Stabilization System Ø 5.5 x 50 mm Cannulated Polyaxial Screw - NT