DBM Putty 5.0cc Syringe

GUDID 00849777009621

ONE (1) PACKAGE - CONTAINING 5.0cc

BACTERIN INTERNATIONAL, INC.

Bone matrix implant, human-derived

• Primary Device ID: 00849777009621
• NIH Device Record Key: 66f007fe-ca2c-4ce4-90aa-708b4a41a0c5
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: DBM Putty 5.0cc Syringe
• Version Model Number: ES395050
• Company DUNS: 829387302
• Company Name: BACTERIN INTERNATIONAL, 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: true
• Device Kit: false
• Device Combination Product: true
• Single Use: true
• Lot Batch: true
• Serial Number: true
• Manufacturing Date: false
• Expiration Date: true
• Donation Id Number: true
• 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	00849777009621 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K130498

FDA Product Code

• MBP: Filler, Bone Void, Osteoinduction (W/O Human Growth Factor)

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: 2019-01-10
• Device Publish Date: 2018-12-10

On-Brand Devices [DBM Putty 5.0cc Syringe ]

• 00849777009621: ONE (1) PACKAGE - CONTAINING 5.0cc
• 00849777008570: ONE (1) PACKAGE - CONTAINING 5.0cc