FDA UDI Not in Commercial Distribution 🇺🇸 United States

Valeo Spacer System

DI: M555111113312 · Model: D · SINTX Technologies, Inc.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
Valeo Spacer System
Primary DI
M555111113312
Version / Model
D
Catalog Number
11.111.3312
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
5
Public Version Date
2026-03-20
Public Version Status
Update
Public Device Record Key
417c7e82-0b0c-482f-a199-0db88c202313
Distribution End Date
2023-09-21

Device Description

Valeo II TL 6° 10x33 12mm

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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
61958 Ceramic spinal interbody fusion cage

Identifiers

Type ID
Primary M555111113312

Customer Contacts

Phone
801-839-3500

Device Sizes

Type Value Unit Text
Outer Diameter 12 Millimeter
Width 33 Millimeter
Length 10 Millimeter