MASTERGRAFT® MATRIX

GUDID 00885074327266

BIOLOGICS 7600305 MSTRGRFT MATRX 5CC KIT

MEDTRONIC SOFAMOR DANEK, INC.

Bone matrix implant, animal-derived, bioabsorbable Bone matrix implant, animal-derived, bioabsorbable

• Primary Device ID: 00885074327266
• NIH Device Record Key: 080578dc-dbf1-4d23-8c27-3b192e357e9a
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: MASTERGRAFT® MATRIX
• Version Model Number: 7600305
• Company DUNS: 830350380
• Company Name: MEDTRONIC SOFAMOR DANEK, 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: false
• 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

Customer Support Contacts

• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com
• Phone: +1(800)633-8766
• Email: Corporate.UDI@medtronic.com

Device Dimensions

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

Device Identifiers

Device Issuing Agency	Device ID
GS1	00885074327266 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K023553

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: 2015-07-20

On-Brand Devices [MASTERGRAFT® MATRIX]

• 00885074327266: BIOLOGICS 7600305 MSTRGRFT MATRX 5CC KIT
• 00885074012308: BIOLOGICS 7600320 MSTRGRFT MATRX 20CC KT
• 00885074012292: BIOLOGICS 7600310 MSTRGRFT MATRX 10CC KT