FDA UDI In Commercial Distribution 🇺🇸 United States

SiNAPTIC Osteotomy Wedge System

DI: G817103151100 · Model: Inserter - Rev. 0 · SINTX Technologies, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
SiNAPTIC Osteotomy Wedge System
Primary DI
G817103151100
Version / Model
Inserter - Rev. 0
Catalog Number
103-15-1100
Company Name
SINTX Technologies, Inc.
Labeler DUNS
028629553
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2026-04-06
Public Version
1
Public Version Date
2026-04-14
Public Version Status
New
Public Device Record Key
770d6001-0317-48cb-af67-935899a40a46

Device Description

Osteotomy Wedge System Wedge Inserter, Inserter Assembly

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
PLF Bone Wedge

GMDN Terms

Code Name
61617 Metallic osteotomy fusion cage, non-customized

Identifiers

Type ID
Primary G817103151100

Premarket Submissions

Submission Number Supplement Number
K252254 000