GUDID 08714729760566

55cm 8 Contact Extension Kit

BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

Spinal cord/peripheral nerve implantable analgesic electrical stimulation system lead extension

• Primary Device ID: 08714729760566
• NIH Device Record Key: 59485e53-38ef-4c9b-8163-4a3e8dc1b6d2
• Commercial Distribution Status: In Commercial Distribution
• Version Model Number: SC-3138-55
• Company DUNS: 824951958
• Company Name: BOSTON SCIENTIFIC NEUROMODULATION 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: true
• Manufacturing Date: false
• 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 Dimensions

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• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	08714729760566 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Approval: P030017

FDA Product Code

• LGW: STIMULATOR, SPINAL-CORD, TOTALLY IMPLANTED FOR PAIN RELIEF

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 4
• Public Version Date: 2024-03-19
• Device Publish Date: 2015-12-14

Devices Manufactured by BOSTON SCIENTIFIC NEUROMODULATION CORPORATION

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• 08714729966357 - Vercise™ Cartesia™ HX: 2024-12-23 Directional Lead Kit, 16 Contact, 30cm
• 08714729966364 - Vercise™ Cartesia™ HX: 2024-12-23 Directional Lead Kit, 16 Contact, 45cm
• 08714729966371 - NA: 2024-12-23 Lead Extension Kit, 2x8 Contact, 55cm
• 08714729966388 - NA: 2024-12-23 Lead Extension Kit, 2x8 Contact, 95cm
• 08714729966395 - NA: 2024-12-23 16 Contact Lead Extension Kit, 55 cm
• 08714729966401 - NA: 2024-12-23 16 Contact Lead Extension Kit, 95 cm