DALI 014.0272

GUDID 00841732121355

Lateral Connector, D6.0 Tulip Head, Round, L20mm

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 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: 00841732121355
• NIH Device Record Key: d38e1365-ea26-406e-a243-9e2a1c4d8f02
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DALI
• Version Model Number: 014.0272
• Catalog Number: 014.0272
• 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: true
• 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

Customer Support Contacts

• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com
• Phone: +1(214)545-5820
• Email: complaints@ctlmed.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00841732121355 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K121568

FDA Product Code

• KWP: APPLIANCE, FIXATION, SPINAL INTERLAMINAL

Sterilization

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

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

[00841732121355]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2024-01-12
• Device Publish Date: 2024-01-04

On-Brand Devices [DALI]

• 00841732128309: 014.0098
• 00841732128293: 014.0097
• 00841732128286: 014.0096
• 00841732128255: 014.0095
• 00841732125209: 014.0030
• 00841732125193: 126.7070
• 00841732125186: 126.7073
• 00841732128026: 126.7070
• 00841732128019: 126.7073
• 00841732143005: Domino Connector, L18mm, D1=6.35, D2=6.35
• 00841732142992: Domino Connector, L16mm, D1=6.35, D2=6.35
• 00841732142985: Lateral Connector, D6.35 Tulip Head, Round, L50mm
• 00841732142978: Lateral Connector, D6.35 Tulip Head, Round, L25mm
• 00841732142961: Lateral Connector, D6.35 Tulip Head, Round, L20mm
• 00841732121386: Lateral Connector, D6.0 Tulip Head, Round, L50mm
• 00841732121379: Lateral Connector, D6.0 Tulip Head, Round, L40mm
• 00841732121362: Lateral Connector, D6.0 Tulip Head, Round, L30mm
• 00841732121355: Lateral Connector, D6.0 Tulip Head, Round, L20mm