FDA UDI In Commercial Distribution 🇺🇸 United States

LSI Arthroereisis Peg

DI: 00819034029488 · Model: TN-LD-9003 · FUSION ORTHOPEDICS, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LSI Arthroereisis Peg
Primary DI
00819034029488
Version / Model
TN-LD-9003
Catalog Number
TN-LD-9003
Company Name
FUSION ORTHOPEDICS, LLC
Labeler DUNS
080307067
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2020-11-24
Public Version
2
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
06eb51b6-f3a1-4ece-90f5-322a16a68868

Device Description

Trial Large

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

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
61246 Surgical implant/trial-implant/sizer holder, single-use

Identifiers

Type ID
Primary 00819034029488

Premarket Submissions

Submission Number Supplement Number
K922292 000