MAUDE Adverse Event Report: MAKO SURGICAL CORP. BOOT ASSEMBLY; STEREOTAXIC DEVICE, ROBOTICS

Model Number	210080
Medical Device Problem Code	Crack (1135)
Health Effect - Clinical Codes	No Patient Involvement (2645); No Known Impact Or Consequence To Patient (2692)
Date of Event	12/20/2019
Type of Reportable Event	Malfunction
Additional Manufacturer Narrative
As part of the normal complaint follow-up, an evaluation of the event has been initiated by mako surgical.A supplemental report will be submitted when additional information becomes available.
Event or Problem Description
Boot is cracked/chipped and could cause sterility problems.Case type: tka.
Event or Problem Description
Boot is cracked/chipped and could cause sterility problems.Case type: tka.
Additional Manufacturer Narrative
Reported issue: boot is cracked/chipped and could cause sterility problems.Product inspection: product inspection was not performed as product was not returned for inspection.Product history review: 1.Review of the device history records indicate (b)(4) devices were manufactured and accepted into final stock on 01/23/2017.No non-conformances were identified during inspection.2.Review of the device history records indicate (b)(4) devices were manufactured and accepted into final stock on 07/24/2017.No non-conformances were identified during inspection.3.Review of the device history records indicate (b)(4) devices were manufactured and rejected on 03/24/2017.A review of (b)(4) revealed the devices were accepted to be used as is on 03/24/2017.The non-conformance is not related to the failure alleged in this compliant.Complaint history review: a review of complaints in catsweb and trackwise related to p/n 210080, l/n 201643112801 shows 2 additional complaints related to the failure in this investigation.Pr id: (b)(6).Conclusion: per (b)(4), preventive maintenance is where an action occurs that identifies device deterioration which may compromise function.Under pm conditions no patient was involved and no actual or potential patient harm existed for the alleged event.The failure could not be determined as the product was not available for inspection.No additional investigation or specific actions are required.If additional information is received then the complaint will be reopened.Corrective action/preventive action: a review of stryker¿s nc/capa database indicated there has been no nc or capa associated with the product and failure mode reported in this event.H3 other text: device not returned.

• Brand Name: BOOT ASSEMBLY
• Common Device Name: STEREOTAXIC DEVICE, ROBOTICS
• Manufacturer (Section D): MAKO SURGICAL CORP.; 2555 davie road; fort lauderdale FL 33317
• MDR Report Key: 9604848
• Report Number: 3005985723-2020-00049
• Device Sequence Number: 19502489
• Product Code: OLO
• UDI-Device Identifier: 00848486031879
• UDI-Public: 00848486031879
• Combination Product (Y/N): N
• Initial Reporter State: IN
• Initial Reporter Country: US
• Number of Events Summarized: 1
• Summary Report (Y/N): N
• Reporter Type: Manufacturer
• Report Source: company representative
• Initial Reporter Occupation: Other
• Type of Report: Initial,Followup
• Report Date (Section B): 03/18/2020

1 Device was Involved in the Event

1 Patient was Involved in the Event

• Is this an Adverse Event Report?: No
• Is this a Product Problem Report?: Yes
• Operator of Device: Health Professional
• Device Model Number: 210080
• Device Catalogue Number: 210080
• Device Lot Number: 201643112801
• Was Device Available for Evaluation?: Yes
• Initial Date Received by Manufacturer: 12/20/2019
• Supplement Date Received by Manufacturer: 02/27/2020
• Initial Report FDA Received Date: 01/19/2020
• Supplement Report FDA Received Date: 03/18/2020
• Is This a Single-Use Device that was Reprocessed and Reused on a Patient? (Y/N): No
• Patient Sequence Number: 1
• Outcome Attributed to Adverse Event: Other