FDA UDI In Commercial Distribution 🇺🇸 United States

Polaris™ 5.5 Spinal System

DI: 00880304987005 · Model: 5006753E · BIOMET SPINE LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Polaris™ 5.5 Spinal System
Primary DI
00880304987005
Version / Model
5006753E
Catalog Number
5006753E
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
5
Public Version Date
2025-07-02
Public Version Status
Update
Public Device Record Key
86b0df3d-2b58-4eb3-a3d1-1d0882f16f70

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

GMDN Terms

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

Identifiers

Type ID
Primary 00880304987005

Customer Contacts

Device Sizes

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