Spirotome Spine SS08SP

GUDID 05407005000250

The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be used in humans to take out adequate samples of soft tissu

Bioncise

Soft-tissue biopsy needle, single-use

• Primary Device ID: 05407005000250
• NIH Device Record Key: 88a9fa6b-8015-41ff-a635-937ee4fffba8
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Spirotome Spine
• Version Model Number: SS08SP
• Catalog Number: SS08SP
• Company DUNS: 371402316
• Company Name: Bioncise
• Device Count: 1
• DM Exempt: false
• Pre-market Exempt: false
• MRI Safety Status: MR Conditional
• Human Cell/Tissue Product: false
• Device Kit: true
• Device Combination Product: false
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: true
• Expiration Date: true
• Donation Id Number: true
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: true
• RX Perscription: true
• OTC Over-The-Counter: false

Device Identifiers

Device Issuing Agency	Device ID
GS1	05407005000250 [Package]; Contains: 05407005001257; Package: Box [5 Units]; In Commercial Distribution
GS1	05407005001257 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K080095

FDA Product Code

• KNW: Instrument, Biopsy

Sterilization

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

Device Entry Metadata

• Public Version Status: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2018-10-01
• Device Publish Date: 2018-08-31

On-Brand Devices [Spirotome Spine]

• 05407005000267: The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be use
• 05407005000250: The Spirotome Biopsy Needle Set is a family of core soft tissue biopsy medical devices to be use