FDA UDI In Commercial Distribution 🇺🇸 United States

iTotal® PS iPoly® XE Insert Kit

DI: M572RPS0201600021 · Model: RPS020160002 · Conformis, Inc.
Product Codes
3
GMDN Terms
2
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
iTotal® PS iPoly® XE Insert Kit
Primary DI
M572RPS0201600021
Version / Model
RPS020160002
Catalog Number
RPS0201600
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
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
6879b6c8-c33e-41c2-b21b-ba703d88bf5a

Device Description

NA

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

GMDN Terms

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

Identifiers

Type ID
Primary M572RPS0201600021

Customer Contacts

Phone
781-345-9001

Device Sizes

Type Value Unit Text
Device Size Text, specify 16mm thick on the medial side, lateral side is patient specific