FDA UDI In Commercial Distribution 🇺🇸 United States

Polaris™ 5.5 Spinal System

DI: 00880304986992 · Model: 5006754E · BIOMET SPINE LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Polaris™ 5.5 Spinal System
Primary DI
00880304986992
Version / Model
5006754E
Catalog Number
5006754E
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-09-30
Public Version
2
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
4c3e8dee-cf77-4d28-a761-a3f62d5fd9c9

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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL
NKB Thoracolumbosacral pedicle screw system
MNI Orthosis, spinal pedicle fixation
MNH Orthosis, spondylolisthesis spinal fixation
KWQ Appliance, fixation, spinal intervertebral body

GMDN Terms

Code Name
61324 Bone-screw internal spinal fixation system, sterile

Identifiers

Type ID
Primary 00880304986992

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Cross Connector, Large