STRATOFUSE

GUDID 00813954025247

Bioactive Putty

COLLAGEN MATRIX, INC.

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

• Primary Device ID: 00813954025247
• NIH Device Record Key: 9fff352d-23d0-451c-a7c9-18cc0946c277
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: STRATOFUSE
• Version Model Number: BA47-000020
• 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 Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0
• Device Size Text, specify: 0

Device Identifiers

Device Issuing Agency	Device ID
GS1	00813954025247 [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: 2022-10-06
• Device Publish Date: 2022-09-28

On-Brand Devices [STRATOFUSE]

• 00813954025247: Bioactive Putty
• 00813954025230: Bioactive Putty
• 00813954025223: Bioactive Putty
• 00813954025216: Bioactive Putty
• 00813954025209: Bioactive Strip
• 00813954025193: Bioactive Strip
• 00813954025186: Bioactive Strip
• 00813954025179: Bioactive Strip
• 00813954025162: Bone Graft Strip