FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal® Posterior Stabilized (PS) Knee Replacement System

DI: M572TPS1211111021 · Model: TPS121111102 · Conformis, Inc.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal® Posterior Stabilized (PS) Knee Replacement System
Primary DI
M572TPS1211111021
Version / Model
TPS121111102
Catalog Number
TPS1211111
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-01-26
Public Version
3
Public Version Date
2022-08-15
Public Version Status
Update
Public Device Record Key
d19f2619-53a0-44be-94f5-6c6b4ee10796

Device Description

ITOTAL PS–IPOLY XE–IMPLANT KIT–LEFT or right

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
OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive
OOG Knee Arthroplasty Implantation System
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

GMDN Terms

Code Name
58910 Total knee prosthesis implantation guide-instrument kit
33665 Posterior-stabilized total knee prosthesis

Identifiers

Type ID
Primary M572TPS1211111021

Customer Contacts

Phone
781-345-9001

Device Sizes

Type Value Unit Text
Device Size Text, specify Patient Specific