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

MAUDE Adverse Event Report: SYNTHES GMBH PLATE 7 HOLE CONDYLAR 95 DEGREE 70MM/124MM; APPLIANCE, FIXATION, NAIL/BLADE/PLATE

  • 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
 

SYNTHES GMBH PLATE 7 HOLE CONDYLAR 95 DEGREE 70MM/124MM; APPLIANCE, FIXATION, NAIL/BLADE/PLATE Back to Search Results
Model Number 23774
Device Problem Break (1069)
Patient Problem Insufficient Information (4580)
Event Date 01/12/2022
Event Type  malfunction  
Event Description
The plate has broken per x-ray (b)(6) 2022, requiring replacement; surgery to be done (b)(6) 2022.One of the screws also broke.Are these items made from steel or titanium? two x-ray pictures uploaded may be of poor quality, taken (b)(6) 2022, one is from 4-week post op follow up, other is from (b)(6) 2022 follow up, per the chart, the implant is: plate 7 hole condylar 95 degree 70mm/124mm, implant type: plate implanted area: femur, laterality: left implanted on: (b)(6) 2021, number implanted:1, implanted by: (b)(6), md implanted at: (b)(6); status: implanted, manufacturer: synthes cmf (formerly maxillofacial) model number: 23774, lot number: na.All 7 self tapping screws (only one broken) are also synthes, models 214.Xxx (last three numbers vary with screw size).Fda safety report id# (b)(4).
 
Search Alerts/Recalls

  New Search  |  Submit an Adverse Event Report

Brand Name
PLATE 7 HOLE CONDYLAR 95 DEGREE 70MM/124MM
Type of Device
APPLIANCE, FIXATION, NAIL/BLADE/PLATE
Manufacturer (Section D)
SYNTHES GMBH
MDR Report Key13307192
MDR Text Key284315587
Report NumberMW5106820
Device Sequence Number1
Product Code LXT
Combination Product (y/n)N
Reporter Country CodeUS
Number of Events Reported1
Summary Report (Y/N)N
Report Source Voluntary
Reporter Occupation Patient
Type of Report Initial
Report Date 01/15/2022
2 Devices were Involved in the Event: 1   2  
1 Patient was Involved in the Event
Date FDA Received01/19/2022
Is this an Adverse Event Report? No
Is this a Product Problem Report? Yes
Device Model Number23774
Was Device Available for Evaluation? Yes
Patient Sequence Number1
Treatment
APPLE CIDER VINEGAR; CALCIUM; CELECOXIB; CITALOPRAM ; CO-Q10; GABAPENTIN ; GLUCOSAMINE/CHONDROITIN; LUTEIN ; MANGANESE ; MSM; NEURIVA; OXYCODONE; SAW PALMETTO; VITAMIN B STRESS COMPLEX ; VITAMIN C; VITAMIN D ; ZEAXANTHIN
Patient Outcome(s) Other;
Patient Age66 YR
Patient SexFemale
Patient Weight91 KG
Patient EthnicityNon Hispanic
Patient RaceWhite
-
-