Identity Imprint PS Knee Replacement System TPS-000-D00F

GUDID M572TPS000D00F021

PS Femoral INSTRUMENTS,ALL SIZES LEFT AND RIGHT

Conformis, Inc.

Total knee prosthesis implantation guide-instrument kit
Primary Device IDM572TPS000D00F021
NIH Device Record Keye1677da2-75f3-4498-baf0-383f35883fa2
Commercial Distribution StatusIn Commercial Distribution
Brand NameIdentity Imprint PS Knee Replacement System
Version Model NumberTPS-000-D00F1
Catalog NumberTPS-000-D00F
Company DUNS808821883
Company NameConformis, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numbertrue
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com
Phone781-345-9001
Emailcustomer-service@conformis.com

Device Dimensions

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Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM572TPS000D00F021 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHProsthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-04
Device Publish Date2024-06-26

Devices Manufactured by Conformis, Inc.

M572TCR000D00F021 - Identity Imprint CR Knee Replacement System2024-07-04 CR FEMORAL INSTRUMENTS,ALL SIZES LEFT AND RIGHT
M572TCR000D00T021 - Identity Imprint CR Knee Replacement System2024-07-04 CR TIBIAL INSTRUMENTS ALL SIZES LEFT OR RIGHT
M572TPS000D00F021 - Identity Imprint PS Knee Replacement System2024-07-04PS Femoral INSTRUMENTS,ALL SIZES LEFT AND RIGHT
M572TPS000D00F021 - Identity Imprint PS Knee Replacement System2024-07-04 PS Femoral INSTRUMENTS,ALL SIZES LEFT AND RIGHT
M572TCR302T07S011 - Identity Imprint Porous CR 2024-02-01 IDENTITY IMPRINT POROUS CR TIBIAL TRAY SIZE 7
00810933031817 - Calcar Planer Adapter Drop-in2023-12-13 Calcar Planer Adapter Drop-in ED-09733
M572POV0123208011 - Identity Imprint Porous CR 2023-09-18 POROUS OVAL PATELLA, 32MM X 8MM, iPoly
M572POV0123509011 - Identity Imprint Porous CR 2023-09-18 POROUS OVAL PATELLA, 35MM X 9MM, iPoly
M572POV0123809011 - Identity Imprint Porous CR 2023-09-18 POROUS OVAL PATELLA, 38MM X 9MM, iPoly

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