contour BA

GUDID 00850009685193

Moldable Bone Graft Matrix

COLLAGEN MATRIX, INC.

Bone matrix implant, animal-derived, bioabsorbable

• Primary Device ID: 00850009685193
• NIH Device Record Key: 86a9a28a-e983-4837-bb11-3007f8b358a1
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: contour BA
• Version Model Number: CBA-1600
• 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 Dimensions

• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00850009685193 [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: New
• Device Record Status: Published
• Public Version Number: 1
• Public Version Date: 2019-11-25
• Device Publish Date: 2019-11-15

On-Brand Devices [contour BA]

• 00850009685193: Moldable Bone Graft Matrix
• 00850009685186: Moldable Bone Graft Matrix
• 00850009685179: Moldable Bone Graft Matrix
• 00850009685162: Moldable Bone Graft Matrix
• 00850009685155: Moldable Bone Graft Matrix
• 00850009685148: Moldable Bone Graft Matrix