MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 03,05 report with the FDA on 2014-10-01 for ITOTAL UNK manufactured by Conformis.
[5094246]
Data presented by dr. (b)(6) in a conference presentation indicated that 6 itotal patients required manipulation under anesthesia to improve post-operative range of motion. One manipulation was unsuccessful and the patient was scheduled for revision for arthrofibrosis.
Patient Sequence No: 1, Text Type: D, B5
[12366606]
Serial number and device model information was not available. Investigation specific to the affected patients and devices could not be conducted.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3004153240-2014-00129 |
MDR Report Key | 4185991 |
Report Source | 03,05 |
Date Received | 2014-10-01 |
Date of Report | 2014-09-03 |
Date Mfgr Received | 2014-09-03 |
Date Added to Maude | 2014-10-21 |
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 | 0 |
Event Location | 0 |
Manufacturer Contact | KARINA SNOW |
Manufacturer Street | 28 CROSBY DR. |
Manufacturer City | BEDFORD MA 01730 |
Manufacturer Country | US |
Manufacturer Postal | 01730 |
Manufacturer Phone | 7813459195 |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ITOTAL |
Generic Name | TOTAL KNEE REPLACEMENT SYSTEM |
Product Code | HSH |
Date Received | 2014-10-01 |
Catalog Number | UNK |
Operator | HEALTH PROFESSIONAL |
Device Availability | N |
Device Age | DA |
Device Eval'ed by Mfgr | R |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | CONFORMIS |
Manufacturer Address | CROSBY DR. BEDFORD MA 01730 US 01730 |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Required No Informationntervention | 2014-10-01 |