OssiMend Putty

GUDID 00813954021164

Bone Graft Matrix, 2cc

COLLAGEN MATRIX, INC.

Bone matrix implant, animal-derived, bioabsorbable

• Primary Device ID: 00813954021164
• NIH Device Record Key: 4d9a10a8-0339-480b-bbae-2c7dcb59a2bd
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: OssiMend Putty
• Version Model Number: MCCP02
• Company DUNS: 176262442
• Company Name: COLLAGEN MATRIX, 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: true
• Donation Id Number: false
• 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	00813954021164 [Primary]

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: 2
• Public Version Date: 2018-03-29
• Device Publish Date: 2015-10-22

On-Brand Devices [OssiMend Putty]

• 00813954022215: Bone Graft Matrix, 10cc
• 00813954022208: Bone Graft Matrix, 5cc
• 00813954022192: Bone Graft Matrix, 2cc
• 00813954021188: Bone Graft Matrix, 10cc
• 00813954021171: Bone Graft Matrix, 5cc
• 00813954021164: Bone Graft Matrix, 2cc
• 00813954026879: Bone Graft Matrix
• 00813954026862: Bone Graft Matrix
• 00813954026855: Bone Graft Matrix