FDA UDI In Commercial Distribution 🇺🇸 United States

Zyston® Straight Interbody Fusion System

DI: 00880304822702 · Model: 14-534678 · BIOMET SPINE LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Zyston® Straight Interbody Fusion System
Primary DI
00880304822702
Version / Model
14-534678
Catalog Number
14-534678
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-06-25
Public Version
3
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
654f67b9-500b-4732-8fc1-483a5f06b9f0

Device Characteristics

Single Use
No
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
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MQP Spinal vertebral body replacement device
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary 00880304822702

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify STR TRIAL 18HX25LX10W CONVEX 10MM WIDE - FIXED