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iTotal® Posterior Stabilized (PS) Knee Replacement System

FDA UDI

Class II (US FDA UDI)

by Conformis, Inc.

Identity

Trade Name
iTotal® Posterior Stabilized (PS) Knee Replacement System FDA UDI
Generic Name
Total knee prosthesis implantation guide-instrument kit FDA UDI
Device Name
ITOTAL PS–IPOLY XE–IMPLANT KIT–LEFT or right FDA UDI
Model / Reference
TPS121111102 FDA UDI
Description
ITOTAL PS–IPOLY XE–IMPLANT KIT–LEFT or right FDA UDI

Identifiers

Catalog Number
TPS1211111 FDA UDI
Primary DI / UDI-DI
M572TPS1211111021 FDA UDI
FDA Product Code
OIY FDA UDI
OOG FDA UDI
JWH FDA UDI
GMDN Term
Total knee prosthesis implantation guide-instrument kit FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

Yes

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

No

FDA UDI

Serial Number

Yes

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI
MRI Safety
MR Conditional FDA UDI

Category: Posterior-stabilized total knee prosthesisTotal knee prosthesis implantation guide-instrument kit

iTotal® Posterior Stabilized (PS) Knee Replacement System by Conformis, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Total knee prosthesis implantation guide-instrument kit.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Conformis, Inc.

Sources (1)

  • FDA UDI d19f2619-53a0-44be-94f5-6c6b4ee10796 36 fields · synced May 31, 2026