Bi-Ostetic Bioactive Glass Foam AA-05P

GUDID 00816125023790

Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralized with hydroxyapatite (HA) – tri-calcium phosphate (TCP) granules and 45S5 bioactive glass granules. The bovine fibrillar collagen component is biocompatible and the 45S5 glass particles are bioactive. Bi-Ostetic Bioactive Glass Foam is indicated for use in bony voids or gaps of the skeletal system (i.e. extremities, pelvis and posterolateral spine). These osseous defects are surgically created or result from traumatic injury to the bone and are not intrinsic to the stability of the bony structure. The graft resorbs and is replaced by the growth of new bone during the healing process. Bi-Ostetic Bioactive Glass Foam must be used with autogenous bone marrow aspirate and autograft in the posterolateral spine.

BERKELEY ADVANCED BIOMATERIALS, LLC

Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial Bone matrix implant, synthetic, non-antimicrobial
Primary Device ID00816125023790
NIH Device Record Keyf1ec4571-dc7a-477f-bab2-80cdcc268777
Commercial Distribution StatusIn Commercial Distribution
Brand NameBi-Ostetic Bioactive Glass Foam
Version Model NumberAA-05P
Catalog NumberAA-05P
Company DUNS081067703
Company NameBERKELEY ADVANCED BIOMATERIALS, LLC
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100816125023790 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MQVFiller, Bone Void, Calcium Compound

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-09-02
Device Publish Date2020-08-25

On-Brand Devices [Bi-Ostetic Bioactive Glass Foam]

00816125023578Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023561Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023530Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023523Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023516Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023509Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023639Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023622Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023806Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023790Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize
00816125023783Bi-Ostetic Bioactive Glass Foam is a bone void filler consisting of a collagen matrix mineralize

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.