FDA UDI Not in Commercial Distribution 🇺🇸 United States

Preference 2

DI: M555286552040 · Model: B · SINTX Technologies, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Preference 2
Primary DI
M555286552040
Version / Model
B
Catalog Number
28-6552-040
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
6
Public Version Date
2026-03-20
Public Version Status
Update
Public Device Record Key
eb240085-5ee6-4ea5-ae3f-032522c662b1
Distribution End Date
2024-10-15

Device Description

ø6.5 Triple Lead Closed Polyaxial Screw Assembly, 40mm

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
No
Sterilization Prior Use
Yes
Sterilization Methods
Radiation Sterilization

Product Codes

Code Name
MNI Orthosis, Spinal Pedicle Fixation
KWP Appliance, Fixation, Spinal Interlaminal
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M555286552040

Customer Contacts

Phone
801-839-3500

Device Sizes

Type Value Unit Text
Length 40 Millimeter
Outer Diameter 6.5 Millimeter