MAUDE Adverse Event Report: MAKO SURGICAL CORP. TIBIAL INSERT ONLAY TRIAL-SIZE 5-8MM; PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYM

Catalog Number 170705-1

Device Problems Break (1069); Detachment Of Device Component (1104); Crack (1135); Fracture (1260); Material Integrity Problem (2978)

Patient Problems No Consequences Or Impact To Patient (2199); No Code Available (3191)

Event Date 07/15/2016

Event Type  malfunction  

Manufacturer Narrative

When completed, the investigation results will be submitted in a supplemental report.

Event Description

Tibial onlay trial insert cracked during impaction of trial components.A small piece of the trial poly broke off.

Manufacturer Narrative

An event regarding crack/fracture involving a tibial insert onlay trial size 5-8mm was reported.The event was confirmed.The device was returned in used condition.There are scratches in various areas of the trial.There is a piece broken off from the right anterior corner of the trial.Examination of the returned device with material analysis engineer indicated the fracture surface was due to overload conditions over multiple impactions and the damage due to impaction.Further assessment is not required.Medical records received and evaluation: not performed as medical records were not provided.Review of the device history records indicates devices were manufactured and accepted into final stock with no reported discrepancies.There have been no other events for this lot.The investigation concluded that crack/fracture was caused by overload conditions during use.The mar team concluded that the, the fracture surface was due to overload conditions and damage due to impaction and further assessment was not required.

Event Description

Tibial onlay trial insert cracked during impaction of trial components.A small piece of the trial poly broke off.

• Brand Name: TIBIAL INSERT ONLAY TRIAL-SIZE 5-8MM
• Type of Device: PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYM
• Manufacturer (Section D): MAKO SURGICAL CORP.; 2555 davie road; fort lauderdale FL 33317
• Manufacturer (Section G): MAKO SURGICAL CORP.; 2555 davie road; fort lauderdale FL 33317
• Manufacturer Contact: keyla colon ; 325 corporate drive; mahwah, NJ 07430 ; 2018315000
• MDR Report Key: 5868303
• MDR Text Key: 52785748
• Report Number: 3005985723-2016-00247
• Device Sequence Number: 1
• Product Code: NPJ
• Combination Product (y/n): N
• Reporter Country Code: US
• PMA/PMN Number: K090763
• Number of Events Reported: 1
• Summary Report (Y/N): N
• Report Source: Manufacturer
• Source Type: company representative
• Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date: 07/15/2016

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Date FDA Received: 08/11/2016
• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Device Operator: Health Professional
• Device Catalogue Number: 170705-1
• Device Lot Number: 12110115
• Was Device Available for Evaluation?: Device Returned to Manufacturer
• Date Returned to Manufacturer: 07/21/2016
• Is the Reporter a Health Professional?: No
• Date Manufacturer Received: 09/19/2016
• Was Device Evaluated by Manufacturer?: Yes
• Is the Device Single Use?: No
• Is This a Reprocessed and Reused Single-Use Device?: No
• Type of Device Usage: Reuse
• Patient Sequence Number: 1
• Patient Outcome(s): Other
• Patient Age: 71 YR