FDA UDI In Commercial Distribution 🇺🇸 United States

SpineTune TL

DI: 03662663007894 · Model: ST6252T-S · LDR Spine Usa, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SpineTune TL
Primary DI
03662663007894
Version / Model
ST6252T-S
Company Name
LDR Spine Usa, Inc.
Labeler DUNS
615789729
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
5
Public Version Date
2022-11-07
Public Version Status
Update
Public Device Record Key
e504580f-aed5-4271-9c80-fce971a5d8e3

Device Description

CANNUL. POLY. SCREW D5.5 L35MM

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation
KWP Appliance, Fixation, Spinal Interlaminal

GMDN Terms

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

Identifiers

Type ID
Primary 03662663007894

Customer Contacts

Phone
512-344-3333

Device Sizes

Type Value Unit Text
Length 35 Millimeter
Outer Diameter 5.5 Millimeter