FDA UDI Not in Commercial Distribution 🇺🇸 United States

Nexgen, Legacy

DI: 00889024305656 · Model: 20-8070-004-02 · Orthosoft Inc
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Nexgen, Legacy
Primary DI
00889024305656
Version / Model
20-8070-004-02
Catalog Number
20-8070-004-02
Company Name
Orthosoft Inc
Labeler DUNS
205670032
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-07
Public Version
5
Public Version Date
2023-01-26
Public Version Status
Update
Public Device Record Key
33051b36-07ba-43f3-8392-a49b2cd20621
Distribution End Date
2020-09-30

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
No
PM Exempt
No
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
OOG Knee Arthroplasty Implantation System
MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
47786 Orthopaedic implant aiming arm

Identifiers

Type ID
Primary 00889024305656

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K131409 000