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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: STELKAST INC. UNICONDYLAR KNEE SYSTEM; UNIKNEE FEMORAL COMPONENT

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STELKAST INC. UNICONDYLAR KNEE SYSTEM; UNIKNEE FEMORAL COMPONENT Back to Search Results
Model Number SC2461-3
Device Problem Insufficient Information (3190)
Patient Problem Unspecified Infection (1930)
Event Date 02/06/2016
Event Type  No Answer Provided  
Manufacturer Narrative
An evaluation of the device cannot be performed as the device was not returned.Should additional information become available, it will be reported in a supplemental report upon completion of the investigation.
 
Event Description
Patient revised due to infection.
 
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Brand Name
UNICONDYLAR KNEE SYSTEM
Type of Device
UNIKNEE FEMORAL COMPONENT
Manufacturer (Section D)
STELKAST INC.
200 hidden valley road
mcmurray PA 15317
Manufacturer (Section G)
STELKAST INC.
200 hidden valley road
mcmurray PA 15317
Manufacturer Contact
john reyher
200 hidden valley road
mcmurray, PA 15317
7249416368
MDR Report Key5978248
MDR Text Key55667436
Report Number2530191-2016-00109
Device Sequence Number1
Product Code HSX
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K032824
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type company representative
Reporter Occupation Medical Equipment Company Technician/Representative
Type of Report Initial
Report Date 09/26/2016
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 Health Professional
Device Model NumberSC2461-3
Device Lot Number34356250619
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Initial Date Manufacturer Received 09/09/2016
Initial Date FDA Received09/26/2016
Was Device Evaluated by Manufacturer? Device Not Returned to Manufacturer
Date Device Manufactured07/07/2015
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 Age63 YR
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