K2M VENADO HA/TCP Cancellous Granules 4815-T0525

GUDID 00816125021567

VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyapatite and 40% beta-tri-calcium phosphate) granules. These materials have been the topic of extensive clinical studies for a several decades. VENADO Granules are safe and have excellent biocompatibility. After it is implanted, the implant resorbs and is later replaced by natural bone. VENADO Granules are a natural choice for sparing patients the trauma of autograft harvesting. It also provides a safe alternative to human or animal cadaver bone that completely eliminates the potential for disease transmission. VENADO Granules are an osteoconductive bone substitute shaped as granules that are intended to be used to fill voids and gaps that are not intrinsic to the stability of the bone structure. These gaps or voids may be located in the extremities, spine, pelvis, or cranium. The granules may be pressed into the void or into the surgical site by hand. The VENADO Granules provide void filling material that acts as a temporary support medium. The granules are not intended to provide structural support during the healing process. The implant is radio-opaque. VENADO Granules are biocompatible and resorbs in the body as bone ingrowth occurs.

BERKELEY ADVANCED BIOMATERIALS, LLC

Bone matrix implant, synthetic

• Primary Device ID: 00816125021567
• NIH Device Record Key: 96b1b122-648b-4972-a814-64a3881e8855
• Commercial Distribution Status: In Commercial Distribution
• Brand Name: K2M VENADO HA/TCP Cancellous Granules
• Version Model Number: 4815-T0525
• Catalog Number: 4815-T0525
• Company DUNS: 081067703
• Company Name: BERKELEY ADVANCED BIOMATERIALS, 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: true
• 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	00816125021567 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

• Premarket Notification: K023703

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: 5
• Public Version Date: 2019-12-23
• Device Publish Date: 2016-04-08

On-Brand Devices [K2M VENADO HA/TCP Cancellous Granules]

• 00816125021628: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021611: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021604: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021598: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021581: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021574: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021567: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap
• 00816125021550: VENADO Granules Bone Graft System is a sterile bone graft comprised of Bi-Ostetic (60% hydroxyap