FDA UDI In Commercial Distribution 🇺🇸 United States

Spine System

DI: 03662663058230 · Model: 14-500779 · BIOMET SPINE LLC
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Spine System
Primary DI
03662663058230
Version / Model
14-500779
Catalog Number
14-500779
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-17
Public Version
5
Public Version Date
2025-07-02
Public Version Status
Update
Public Device Record Key
32a23148-5679-40c5-bbd5-879a883aa253

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

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 03662663058230

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify DOMINO, SS 4.75MMX6.35MM AXIAL