FDA UDI In Commercial Distribution 🇺🇸 United States

FIBERGRAFT BG Matrix

DI: 00856879006229 · Model: 5500-0030 · Prosidyan, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
FIBERGRAFT BG Matrix
Primary DI
00856879006229
Version / Model
5500-0030
Catalog Number
55000030
Company Name
Prosidyan, Inc.
Labeler DUNS
963425488
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-07
Public Version
7
Public Version Date
2023-04-14
Public Version Status
Update
Public Device Record Key
327753bf-7337-4295-b7fd-001a6e43dbd6

Device Description

BG Matrix Bone Graft Substitute, Small, 3cc

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MQV Filler, Bone Void, Calcium Compound

GMDN Terms

Code Name
17751 Bone matrix implant, synthetic, non-antimicrobial

Identifiers

Type ID
Primary 00856879006229

Customer Contacts

Phone
9085173666

Premarket Submissions

Submission Number Supplement Number
K171284 000