FDA UDI In Commercial Distribution 🇺🇸 United States

LSI Arthroereisis Peg

DI: 00840124519503 · Model: TN-LD-6003 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LSI Arthroereisis Peg
Primary DI
00840124519503
Version / Model
TN-LD-6003
Catalog Number
TN-LD-6003
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2025-05-15
Public Version
1
Public Version Date
2025-05-23
Public Version Status
New
Public Device Record Key
18263cb3-3d63-4cc1-af54-ed7b44ffddff

Device Description

Large Drill Guide

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
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
Yes

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MJW Prosthesis, Subtalar, Plug, Polymer

GMDN Terms

Code Name
57789 Surgical drill guide, single-use

Identifiers

Type ID
Primary 00840124519503