FDA UDI In Commercial Distribution 🇺🇸 United States

Duo Expandable Interbody Fusion System

DI: M7408605433 · Model: 86-05-43-3 · SPINEOLOGY INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Duo Expandable Interbody Fusion System
Primary DI
M7408605433
Version / Model
86-05-43-3
Catalog Number
860-5433
Company Name
SPINEOLOGY INC.
Labeler DUNS
033014361
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-12-29
Public Version
1
Public Version Date
2024-01-08
Public Version Status
New
Public Device Record Key
0d2e7c79-3edc-4490-8bd5-f90f6c419540

Device Description

160mm Fixation Pin

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
MR Unsafe
Direct Marking Exempt
No
PM Exempt
Yes
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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary M7408605433

Customer Contacts

Phone
651-256-8500