• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

MAUDE Adverse Event Report: K2M, INC. DEFORMITY, UNIPLANAR SCREW; SIZE 6.5X45 MM; THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM

  • Print
  • Share
  • E-mail
-
Super Search Devices@FDA
510(k) | DeNovo | Registration & Listing | Adverse Events | Recalls | PMA | HDE | Classification | Standards
CFR Title 21 | Radiation-Emitting Products | X-Ray Assembler | Medsun Reports | CLIA | TPLC
 

K2M, INC. DEFORMITY, UNIPLANAR SCREW; SIZE 6.5X45 MM; THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM Back to Search Results
Model Number 801-36545M
Device Problem Migration (4003)
Patient Problem Nerve Damage (1979)
Event Date 10/08/2020
Event Type  Injury  
Event Description
It was reported that a rod slipped out of the head of a mesa deformity uniplanar screw one year post-operatively.Due to the failure, the "exiting nerve root" was compressed.Revision surgery has been performed and the screw has been replaced.
 
Manufacturer Narrative
Updated d9 as product was returned on 12/10/2020.
 
Event Description
It was reported that a rod slipped out of the head of a mesa deformity uniplanar screw one year post-operatively.Due to the failure, the "exiting nerve root" was compressed.Revision surgery has been performed and the screw has been replaced.
 
Manufacturer Narrative
D.4.Lot number has been updated from 'hmhr' to 'hnhr'.Visual inspection: the device was inspected, and it was observed that the screw was positioned in the locked state; however, the inner collet was not completely flush with the outer collet.Analysis of the provided radiological images confirmed that rod slippage had occurred at the distal end of the construct.Functional inspection: some resistance was experienced during locking/unlocking.Device and complaint history records were reviewed for this lot, and no relevant manufacturing issues or similar complaints were identified.Per mesa surgical technique: these internal fixation devices are load sharing devices which maintain alignment until healing occurs.If healing is delayed or does not occur, the implant could eventually break, bend, or loosen.Incidence of pseudoarthrosis could allow for continued dynamic motion within the construct, leading to the axial slip along the rod.Upon review of the part, it was observed that the screw was positioned in the locked state; however, the inner collet was not completely flush with the outer collet.Analysis of the provided radiological images confirmed that rod slippage had occurred at the distal end of the construct.It is possible that non-union contributed to the failure.
 
Event Description
It was reported that a rod slipped out of the head of a mesa deformity uniplanar screw one year post-operatively.Due to the failure, the "exiting nerve root" was compressed.Revision surgery has been performed and the screw has been replaced.
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
DEFORMITY, UNIPLANAR SCREW; SIZE 6.5X45 MM
Type of Device
THORACOLUMBOSACRAL PEDICLE SCREW SYSTEM
Manufacturer (Section D)
K2M, INC.
600 hope parkway se
leesburg VA 20175
MDR Report Key10824971
MDR Text Key215906133
Report Number3004774118-2020-00302
Device Sequence Number1
Product Code NKB
UDI-Device Identifier10888857140301
UDI-Public10888857140301
Combination Product (y/n)N
PMA/PMN Number
K141873
Number of Events Reported1
Summary Report (Y/N)N
Report Source Manufacturer
Source Type distributor
Type of Report Initial,Followup,Followup
Report Date 02/04/2021
1 Device was Involved in the Event
1 Patient was Involved in the Event
Date FDA Received11/11/2020
Is this an Adverse Event Report? Yes
Is this a Product Problem Report? Yes
Device Operator Health Professional
Device Model Number801-36545M
Device Catalogue Number801-36545M
Device Lot NumberHNHR
Was Device Available for Evaluation? Device Returned to Manufacturer
Date Returned to Manufacturer12/10/2020
Date Manufacturer Received01/14/2021
Is This a Reprocessed and Reused Single-Use Device? No
Patient Sequence Number1
Patient Outcome(s) Required Intervention;
Patient Age30 YR
-
-