FDA UDI Not in Commercial Distribution 🇺🇸 United States

Taurus Pedicle Screw System

DI: M555502000001 · Model: C · SINTX Technologies, Inc.
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Taurus Pedicle Screw System
Primary DI
M555502000001
Version / Model
C
Catalog Number
50-2000-001
Company Name
SINTX Technologies, Inc.
Labeler DUNS
028629553
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2017-12-29
Public Version
7
Public Version Date
2026-03-20
Public Version Status
Update
Public Device Record Key
6fa5c618-cdc1-42f1-bd42-d9c3597d1dc6
Distribution End Date
2023-09-13

Device Description

Probe, Sounder, Curved

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
Yes
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
MNI Orthosis, Spinal Pedicle Fixation
MNH Orthosis, Spondylolisthesis Spinal Fixation

GMDN Terms

Code Name
64192 Internal spinal fixation procedure kit, reusable

Identifiers

Type ID
Primary M555502000001

Customer Contacts

Phone
801-839-3500