FDA UDI In Commercial Distribution 🇺🇸 United States

Solitaire™ Anterior Spinal System

DI: 00888480185697 · Model: 1400-1202 · BIOMET SPINE LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Solitaire™ Anterior Spinal System
Primary DI
00888480185697
Version / Model
1400-1202
Catalog Number
1400-1202
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
4
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
7e24fbe8-b674-40fe-a8f4-92e0c9b6b744

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
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
MAX Intervertebral fusion device with bone graft, lumbar
MQP SPINAL VERTEBRAL BODY REPLACEMENT DEVICE

GMDN Terms

Code Name
34170 Vertebral body prosthesis

Identifiers

Type ID
Primary 00888480185697

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify SOLITAIRE NARROW 12MM / 12°