TAURUS

GUDID 00841732144071

T20, CROSS CONNECTOR MANIPULATOR SHORT

CTL MEDICAL CORPORATION

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 Bone-screw internal spinal fixation system, non-sterile

• Primary Device ID: 00841732144071
• NIH Device Record Key: d81151b1-5c29-4e60-ae19-4212e01253f8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: TAURUS
• Version Model Number: 059.7275
• Company DUNS: 080138504
• Company Name: CTL MEDICAL CORPORATION
• 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: false
• Lot Batch: true
• Serial Number: false
• Manufacturing Date: true
• Expiration Date: false
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: false
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732144071 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K162160

FDA Product Code

• MNH: Orthosis, Spondylolisthesis Spinal Fixation

Sterilization

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

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

[00841732144071]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2023-09-21
• Device Publish Date: 2023-09-13

On-Brand Devices [TAURUS]

• 00841732128712: 059.7050
• 00841732128705: 059.7045
• 00841732150928: 5.5mm Straight Rod 600mm CoCr external hex
• 00841732150911: 5.5mm Straight Rod 450mm CoCr external hex
• 00841732150904: 5.5mm Straight Rod 350mm CoCr external hex
• 00841732150898: 5.5mm Straight Rod 250mm CoCr external hex
• 00841732150881: 5.5mm Straight Rod 150mm CoCr external hex
• 00841732150874: 5.5mm Straight Rod 600mm Ti Alloy external hex
• 00841732150867: 5.5mm Straight Rod 450mm Ti Alloy external hex
• 00841732150850: 5.5mm Straight Rod 350mm Ti Alloy
• 00841732150843: 5.5mm Straight Rod 250mm Ti Alloy
• 00841732150836: 5.5mm Straight Rod 50mm Ti Alloy
• 00841732150829: 5.5mm Straight Rod 40mm Ti Alloy
• 00841732150812: 5.5mm Straight Rod 30mm Ti Alloy
• 00841732150805: 5.5mm Curved Rod 250mm Ti Alloy
• 00841732150799: 5.5mm Curved Rod 130mm Ti Alloy
• 00841732150782: 5.5mm Curved Rod 120mm Ti Alloy
• 00841732150775: 5.5mm Curved Rod 110mm Ti Alloy
• 00841732150768: 5.5mm Curved Rod 100mm Ti Alloy
• 00841732150751: 5.5mm Curved Rod 90mm Ti Alloy
• 00841732150744: 5.5mm Curved Rod 85mm Ti Alloy
• 00841732150737: 5.5mm Curved Rod 80mm Ti Alloy
• 00841732150720: 5.5mm Curved Rod 75mm Ti Alloy
• 00841732150713: 5.5mm Curved Rod 70mm Ti Alloy
• 00841732150706: 5.5mm Curved Rod 65mm Ti Alloy
• 00841732150690: 5.5mm Curved Rod 60mm Ti Alloy
• 00841732150683: 5.5mm Curved Rod 55mm Ti Alloy
• 00841732150676: 5.5mm Curved Rod 50mm Ti Alloy
• 00841732150669: 5.5mm Curved Rod 45mm Ti Alloy
• 00841732150652: 5.5mm Curved Rod 40mm Ti Alloy
• 00841732150645: 5.5mm Curved Rod 35mm Ti Alloy
• 00841732150638: 5.5mm Curved Rod 30mm Ti Alloy
• 00841732150492: Screw, Pedicle DL Cannulated, Ø7.5x60mm
• 00841732150485: Screw, Pedicle DL Cannulated, Ø7.5x55mm
• 00841732150478: Screw, Pedicle DL Cannulated, Ø7.5x50mm
• 00841732150461: Screw, Pedicle DL Cannulated, Ø7.5x45mm
• 00841732150454: Screw, Pedicle DL Cannulated, Ø7.5x40mm
• 00841732150447: Screw, Pedicle DL Cannulated, Ø7.5x35mm
• 00841732150430: Screw, Pedicle DL Cannulated, Ø7.5x30mm
• 00841732150423: Screw, Pedicle DL Cannulated, Ø6.5x60mm
• 00841732150416: Screw, Pedicle DL Cannulated, Ø6.5x55mm
• 00841732150409: Screw, Pedicle DL Cannulated, Ø6.5x50mm
• 00841732150393: Screw, Pedicle DL Cannulated, Ø6.5x45mm
• 00841732150386: Screw, Pedicle DL Cannulated, Ø6.5x40mm
• 00841732150379: Screw, Pedicle DL Cannulated, Ø6.5x35mm
• 00841732150362: Screw, Pedicle DL Cannulated, Ø6.5x30mm
• 00841732150355: Screw, Pedicle DL Cannulated, Ø5.5x55mm
• 00841732150348: Screw, Pedicle DL Cannulated, Ø5.5x50mm
• 00841732150331: Screw, Pedicle DL Cannulated, Ø5.5x45mm
• 00841732150324: Screw, Pedicle DL Cannulated, Ø5.5x40mm