AttraX

GUDID 00887517241535

AttraX® Putty, 2cc US

Nuvasive, Inc.

Bone matrix implant, synthetic

• Primary Device ID: 00887517241535
• NIH Device Record Key: b8bd5cf7-08e0-4264-a1cf-d55a07c265b4
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: AttraX
• Version Model Number: 5015002
• Company DUNS: 053950783
• Company Name: Nuvasive, Inc.
• 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: true
• Donation Id Number: false
• Contains Natural Rubber Latex: false
• Labeled No Natural Rubber Latex: false
• RX Perscription: true
• OTC Over-The-Counter: false

Customer Support Contacts

• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com
• Phone: +1(858)909-1800
• Email: RA_UDI@nuvasive.com

Device Identifiers

Device Issuing Agency	Device ID
GS1	00887517241535 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K090641
• Premarket Notification: K151584

FDA Product Code

• MQV: FILLER, BONE VOID, CALCIUM COMPOUND

Sterilization

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

Device Entry Metadata

• Public Version Status: Update
• Device Record Status: Published
• Public Version Number: 3
• Public Version Date: 2018-07-06
• Device Publish Date: 2016-03-29

On-Brand Devices [AttraX]

• 00887517241566: AttraX® Putty, 10cc US
• 00887517241559: AttraX® Putty, 6cc US
• 00887517241542: AttraX® Putty, 5cc US
• 00887517241535: AttraX® Putty, 2cc US
• 00887517241528: AttraX® Putty, 1cc US
• 00887517940025: AttraX Scaffold Strips, Large
• 00887517940018: AttraX Scaffold Strips, Small
• 00887517940001: AttraX Scaffold Blocks, Extra Large
• 00887517939999: AttraX Scaffold Blocks, Large
• 00887517939982: AttraX Scaffold Blocks, Small
• 00887517939975: AttraX Scaffold Morsels, 30cc
• 00887517939968: AttraX Scaffold Morsels, 20cc
• 00887517939951: AttraX Scaffold Morsels, 10cc