FDA UDI In Commercial Distribution 🇺🇸 United States

Fusion™ Posterior Instrument Set

DI: 00840311262632 · Model: 30-FUNNEL · Xtant Medical Holdings, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
Fusion™ Posterior Instrument Set
Primary DI
00840311262632
Version / Model
30-FUNNEL
Company Name
Xtant Medical Holdings, Inc.
Labeler DUNS
081224143
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-12-11
Public Version
1
Public Version Date
2025-12-19
Public Version Status
New
Public Device Record Key
1549c125-6a09-48cc-bb30-71040d76e5a6

Device Description

VBR, Graft Funnel

Device Characteristics

Single Use
No
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
Yes
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
44759 General internal orthopaedic fixation system implantation kit

Identifiers

Type ID
Primary 00840311262632
Previous 00846468031992

Customer Contacts

Phone
888-886-9354