FDA UDI In Commercial Distribution 🇺🇸 United States

Vitality®

DI: 00880304854086 · Model: 07.02047.053 · BIOMET SPINE LLC
Product Codes
6
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Vitality®
Primary DI
00880304854086
Version / Model
07.02047.053
Catalog Number
07.02047.053
Company Name
BIOMET SPINE LLC
Labeler DUNS
018577570
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-06-30
Public Version
2
Public Version Date
2022-03-10
Public Version Status
Update
Public Device Record Key
03801d53-8271-45bd-91c1-36d53220998c

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

GMDN Terms

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

Identifiers

Type ID
Primary 00880304854086

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify Uniplanar Reduction Screw, Ø6.0mm X 40mm