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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: CONFORMIS, INC. IUNI G2; UNICONDYLAR KNEE REPLACEMENT SYSTEM

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CONFORMIS, INC. IUNI G2; UNICONDYLAR KNEE REPLACEMENT SYSTEM Back to Search Results
Catalog Number M5722INT0600220
Device Problem Insufficient Information (3190)
Patient Problem No Information (3190)
Event Date 08/01/2015
Event Type  Injury  
Manufacturer Narrative
Revision surgery is planned for patient with a unicondylar knee implant.Reason for revision is unknown at this time.Review of the device history record indicates that the device was manufactured to specification.
 
Event Description
Revision surgery is planned for patient with a unicondylar knee implant.Reason for revision is unknown at this time.
 
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Brand Name
IUNI G2
Type of Device
UNICONDYLAR KNEE REPLACEMENT SYSTEM
Manufacturer (Section D)
CONFORMIS, INC.
28 crosby drive
bedford MA 01730
Manufacturer Contact
karina snow
28 crosby drive
bedford, MA 01730
7813459195
MDR Report Key5036604
MDR Text Key24355740
Report Number3004153240-2015-00163
Device Sequence Number1
Product Code HSX
Combination Product (y/n)N
Reporter Country CodeGM
PMA/PMN Number
K111916
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type health professional
Reporter Occupation Physician
Report Date 08/27/2015
1 Device was Involved in the Event
1 Patient was Involved in the Event
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Physician
Device Expiration Date08/31/2014
Device Catalogue NumberM5722INT0600220
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? Yes
Initial Date Manufacturer Received Not provided
Initial Date FDA Received08/27/2015
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured03/13/2014
Is the Device Single Use? Yes
Is This a Reprocessed and Reused Single-Use Device? No
Type of Device Usage Initial
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age57 YR
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