MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a health professional,other report with the FDA on 2019-09-10 for MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 8 MM 180734-1 manufactured by Mako Surgical Corp..
Report Number | 3005985723-2019-00658 |
MDR Report Key | 8980990 |
Report Source | HEALTH PROFESSIONAL,OTHER |
Date Received | 2019-09-10 |
Date of Report | 2019-09-10 |
Date of Event | 2019-08-14 |
Date Mfgr Received | 2019-08-14 |
Device Manufacturer Date | 2017-09-07 |
Date Added to Maude | 2019-09-10 |
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. BRAD CURTIS |
Manufacturer Street | 325 CORPORATE DRIVE |
Manufacturer City | MAHWAH NJ 07430 |
Manufacturer Country | US |
Manufacturer Postal | 07430 |
Manufacturer Phone | 2018315000 |
Manufacturer G1 | STRYKER ORTHOPAEDICS-MAHWAH |
Manufacturer Street | 325 CORPORATE DRIVE |
Manufacturer City | MAHWAH NJ 07430 |
Manufacturer Country | US |
Manufacturer Postal Code | 07430 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | MAKO X3 UNI ONLAY TIBIAL INSERT SIZE 4 - 8 MM |
Generic Name | PROSTHESIS, KNEE PATELLOFEMOROTIBIAL, PARTIAL, SEMI-CONSTRAINED, CEMENTED, POLYM |
Product Code | NPJ |
Date Received | 2019-09-10 |
Catalog Number | 180734-1 |
Lot Number | R474R9 |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Eval'ed by Mfgr | R |
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; 2. Required No Informationntervention | 2019-09-10 |