Katana

GUDID 00840606184830

Posterior Access Guide, SS

SPINAL ELEMENTS, INC.

Orthopaedic prosthesis implantation positioning instrument, reusable

• Primary Device ID: 00840606184830
• NIH Device Record Key: b612430c-486b-4ef4-8987-7fe5b75e33a3
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Katana
• Version Model Number: 81046-000
• Company DUNS: 610712213
• Company Name: SPINAL ELEMENTS, INC.
• Device Count: 1
• DM Exempt: true
• Pre-market Exempt: true
• 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: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	00840606184830 [Primary]

FDA Product Code

• LXH: Orthopedic Manual Surgical Instrument

Sterilization

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

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

[00840606184830]

Moist Heat or Steam Sterilization

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2025-05-29
• Device Publish Date: 2025-05-21

On-Brand Devices [Katana]

• 00840606154321: KATANA TM ARM TRAY TOP INSERT
• 00840606154314: KATANA TM ARM TRAY BOTTOM INSERT
• 00840606154307: KATANA TM ARM TRAY LID
• 00840606154291: KATANA TM ARM TRAY BASE
• 00840606154284: KATANA TM ARM TRAY ASSEMBLY
• 00840606161855: LUCENT® L KATANA CENTER BLADE, 180MM
• 00840606161848: LUCENT® L KATANA CENTER BLADE, 170MM
• 00840606161831: LUCENT® L KATANA CENTER BLADE, 160MM
• 00840606161824: LUCENT® L KATANA CENTER BLADE, 150MM
• 00840606161817: LUCENT® L KATANA CENTER BLADE, 140MM
• 00840606161800: LUCENT® L KATANA CENTER BLADE, 130MM
• 00840606161794: LUCENT® L KATANA CENTER BLADE, 120MM
• 00840606161787: LUCENT® L KATANA CENTER BLADE, 110MM
• 00840606161770: LUCENT® L KATANA CENTER BLADE, 100MM
• 00840606161763: LUCENT® L KATANA CENTER BLADE, 90MM
• 00840606161756: LUCENT® L KATANA CENTER BLADE, 80MM
• 00840606184830: Posterior Access Guide, SS
• 00840606184823: Anterior Access Guide, SS