Identity Imprint CR Knee Replacement System TCR-000-D00F

GUDID M572TCR000D00F021

CR FEMORAL INSTRUMENTS,ALL SIZES LEFT AND RIGHT

Conformis, Inc.

Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit Total knee prosthesis implantation guide-instrument kit
Primary Device IDM572TCR000D00F021
NIH Device Record Key52b81c47-f275-4907-abe5-7b4fa7db4788
Commercial Distribution StatusIn Commercial Distribution
Brand NameIdentity Imprint CR Knee Replacement System
Version Model NumberTCR-000-D00F1
Catalog NumberTCR-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

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM572TCR000D00F021 [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

On-Brand Devices [Identity Imprint CR Knee Replacement System]

M572TCR000D00T021CR TIBIAL INSTRUMENTS ALL SIZES LEFT OR RIGHT
M572TCR000D00F021CR FEMORAL INSTRUMENTS,ALL SIZES LEFT AND RIGHT

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