FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal PS

DI: M572RPS0201700121 · Model: RPS-020-170012 · Conformis, Inc.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal PS
Primary DI
M572RPS0201700121
Version / Model
RPS-020-170012
Catalog Number
RPS-020-1700
Company Name
Conformis, Inc.
Labeler DUNS
808821883
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-08-17
Public Version
1
Public Version Date
2022-08-25
Public Version Status
New
Public Device Record Key
2aef39e4-db56-4e94-bb5c-15efdc941fe9

Device Description

ITOTAL PS IPOLY XE - 17MM INSERT - LEFT or right NO TRIAL

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
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
OIY Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer + Additive/Metal/Polymer + Additive

GMDN Terms

Code Name
46585 Tibial insert

Identifiers

Type ID
Primary M572RPS0201700121

Customer Contacts

Phone
781-345-9001

Premarket Submissions

Submission Number Supplement Number
K140833 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Thickness 17mm