FDA UDI In Commercial Distribution 🇺🇸 United States

Virata

DI: 10889981375003 · Model: TL1-30075060 · Seaspine Orthopedics Corporation
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Virata
Primary DI
10889981375003
Version / Model
TL1-30075060
Catalog Number
TL1-30075060
Company Name
Seaspine Orthopedics Corporation
Labeler DUNS
079840876
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-09-26
Public Version
2
Public Version Date
2025-10-24
Public Version Status
Update
Public Device Record Key
f5630617-2498-40e9-9082-df4d8ef4b52e

Device Description

Shank, 7.5mm X 60mm

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
KWP APPLIANCE, FIXATION, SPINAL INTERLAMINAL

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 10889981375003

Premarket Submissions

Submission Number Supplement Number
K250908 000