MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative report with the FDA on 2020-03-23 for 3.0 RIO? ROBOTIC ARM - MICS 209999 manufactured by Mako Surgical Corp..
[184484667]
As part of 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.
Patient Sequence No: 1, Text Type: N, H10
[184484668]
Case number: (b)(4). Case description: (b)(4)- mps reported arm shaking during bone prep. Case type : tka. Update: any surgical delay? If yes ,by how long the surgery was delayed? 15 min. Any patient harm? State any adverse consequences. No. Any medical intervention? No. Was procedure completed manually? The distal femoral cut was completed manually.
Patient Sequence No: 1, Text Type: D, B5
Report Number | 3005985723-2020-00170 |
MDR Report Key | 9865014 |
Report Source | COMPANY REPRESENTATIVE |
Date Received | 2020-03-23 |
Date of Report | 2020-03-23 |
Date of Event | 2020-02-26 |
Date Mfgr Received | 2020-02-26 |
Date Added to Maude | 2020-03-23 |
Event Key | 0 |
Report Source Code | Manufacturer report |
Manufacturer Link | Y |
Number of Patients in Event | 0 |
Adverse Event Flag | 3 |
Product Problem Flag | 3 |
Reprocessed and Reused Flag | 3 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 3 |
Event Location | 3 |
Manufacturer Contact | MR. ALESSANDRA CHAVEZ |
Manufacturer Street | 2555 DAVIE ROAD |
Manufacturer City | FORT LAUDERDALE FL 33317 |
Manufacturer Country | US |
Manufacturer Postal | 33317 |
Manufacturer Phone | 9546280700 |
Manufacturer G1 | MAKO SURGICAL CORP. |
Manufacturer Street | 2555 DAVIE ROAD |
Manufacturer City | FORT LAUDERDALE FL 33317 |
Manufacturer Country | US |
Manufacturer Postal Code | 33317 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | 3.0 RIO? ROBOTIC ARM - MICS |
Generic Name | STEREOTAXIC DEVICE, ROBOTICS |
Product Code | OLO |
Date Received | 2020-03-23 |
Model Number | 209999 |
Catalog Number | 209999 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | MAKO SURGICAL CORP. |
Manufacturer Address | 2555 DAVIE ROAD FORT LAUDERDALE FL 33317 US 33317 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Hospitalization | 2020-03-23 |