FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal® PS

DI: M572RPS0101400021 · Model: RPS010140002 · Conformis, Inc.
Product Codes
2
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal® PS
Primary DI
M572RPS0101400021
Version / Model
RPS010140002
Catalog Number
RPS0101400
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-10-24
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
f59cb758-fd92-43ea-ad69-2192be33f3fb

Device Description

iTotal® Posterior Stabilized (PS) Knee Insert Kit

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
Direct Marking Exempt
No
PM Exempt
No
Has Serial Number
Yes
Has Lot/Batch Number
No
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer
OOG Knee Arthroplasty Implantation System

GMDN Terms

Code Name
46585 Tibial insert
58910 Total knee prosthesis implantation guide-instrument kit

Identifiers

Type ID
Primary M572RPS0101400021

Customer Contacts

Device Sizes

Type Value Unit Text
Height 14 Millimeter