Putty Syringe 5.0cc NB2699

GUDID 00813909011134

Synthetic bone void filler for orthopedic applications

NOVABONE PRODUCTS, LLC

Bone matrix implant, synthetic Bone matrix implant, synthetic

• Primary Device ID: 00813909011134
• NIH Device Record Key: 6f1701ab-1bb9-441a-9e8b-650d81d7254b
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: Putty Syringe 5.0cc
• Version Model Number: NB2699
• Catalog Number: NB2699
• Company DUNS: 828813290
• Company Name: NOVABONE PRODUCTS, LLC
• 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: 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 Dimensions

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

Operating and Storage Conditions

• Storage Environment Temperature: Between 0 Degrees Celsius and 40 Degrees Celsius
• Storage Environment Temperature: Between 0 Degrees Celsius and 40 Degrees Celsius

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813909011134 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K082672

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: 2016-03-07

On-Brand Devices [Putty Syringe 5.0cc]

• 00813909011134: Synthetic bone void filler for orthopedic applications
• 00813909011110: Synthetic bone void filler for orthopedic applications
• 00813909012810: Synthetic bone void filler for orthopedic applications