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U.S. Department of Health and Human Services

MAUDE Adverse Event Report: SMITH & NEPHEW, INC. REF SPHER HEAD SCREW 35MM; PRSTHSS,HP,SMCNSTRND,UNCMNTD,MTLPLYMR,NNPRS,CLICMPHSPHT

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SMITH & NEPHEW, INC. REF SPHER HEAD SCREW 35MM; PRSTHSS,HP,SMCNSTRND,UNCMNTD,MTLPLYMR,NNPRS,CLICMPHSPHT Back to Search Results
Catalog Number 71332535
Device Problem Insufficient Information (3190)
Patient Problem Injury (2348)
Event Date 11/27/2017
Event Type  Injury  
Event Description
It was reported that a revision surgery was performed due to uknown reasons.
 
Manufacturer Narrative
The associated complaint device was not returned for evaluation.[(b)(4)].
 
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Brand Name
REF SPHER HEAD SCREW 35MM
Type of Device
PRSTHSS,HP,SMCNSTRND,UNCMNTD,MTLPLYMR,NNPRS,CLICMPHSPHT
Manufacturer (Section D)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
Manufacturer (Section G)
SMITH & NEPHEW, INC.
1450 brooks road
memphis TN 38116
Manufacturer Contact
markus poettker
1450 brooks road
memphis, TN 38116
MDR Report Key7140050
MDR Text Key95550996
Report Number1020279-2017-01325
Device Sequence Number1
Product Code MEH
UDI-Device Identifier03596010463289
UDI-Public03596010463289
Combination Product (y/n)N
Reporter Country CodeUS
PMA/PMN Number
K990666
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type consumer
Reporter Occupation Patient
Type of Report Initial,Followup
Report Date 03/15/2018
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received12/21/2017
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? No
Device Operator Health Professional
Device Expiration Date02/26/2020
Device Catalogue Number71332535
Device Lot Number10BT39685
Was Device Available for Evaluation? No
Is the Reporter a Health Professional? No
Date Manufacturer Received11/28/2017
Was Device Evaluated by Manufacturer? No
Date Device Manufactured02/28/2010
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) Hospitalization; Required Intervention;
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