Cordera Hip System (Stainless Steel) Trial Neck 127degree, 29.0mm 1080-651

GUDID 00810933031145

(Stainless Steel)Trial Neck 127degree, 29.0mm

Conformis, Inc.

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Primary Device ID00810933031145
NIH Device Record Keyb6e77ca5-8d62-40da-838a-cf8c82053e51
Commercial Distribution StatusIn Commercial Distribution
Brand NameCordera Hip System (Stainless Steel) Trial Neck 127degree, 29.0mm
Version Model Number1080-651
Catalog Number1080-651
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 Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
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

Device Dimensions

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Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100810933031145 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

LPHProsthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


[00810933031145]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-03-15
Device Publish Date2022-03-07

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M572POV0124110011 - Identity Imprint Porous CR 2023-09-18 POROUS OVAL PATELLA, 41MM X 10MM, iPoly
M572POV0124411011 - Identity Imprint Porous CR 2023-09-18 POROUS OVAL PATELLA, 44MM X 11MM, iPoly
M572TCR102F01S011 - Identity Imprint Porous CR2023-09-18 POROUS CR FEMORAL IMPLANT SIZE 1 LEFT OR RIGHT

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