MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a 07 report with the FDA on 2013-05-06 for ARTELON CMC SPACER manufactured by Artimplant Ab.
[18851425]
Explantation of artelon stt spacer due to increasing pain at activity. The patient had been pain free and functional until approx 18 months after implant surgery. X-rays revealed recurrent osteophytes. (same patient as 3004878714-2013-00013). (b)(4).
Patient Sequence No: 1, Text Type: D, B5
[19211928]
Explant sent for histological analysis. No result yet.
Patient Sequence No: 1, Text Type: N, H10
Report Number | 3004878714-2013-00014 |
MDR Report Key | 3161564 |
Report Source | 07 |
Date Received | 2013-05-06 |
Date of Report | 2013-05-28 |
Date of Event | 2013-05-07 |
Date Mfgr Received | 2013-05-07 |
Date Added to Maude | 2013-06-12 |
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 | 0 |
Health Professional | 3 |
Initial Report to FDA | 3 |
Report to FDA | 0 |
Event Location | 0 |
Manufacturer Street | HULDA MELLGRENS GATA 5 |
Manufacturer City | V. FROLUNDA SE-421 32 |
Manufacturer Country | SW |
Manufacturer Postal | SE-421 32 |
Manufacturer Phone | 17465600 |
Manufacturer G1 | ARTIMPLANT AB |
Manufacturer Street | HULDA MELLGRENS GATA 5 |
Manufacturer City | V. FROLUNDA |
Manufacturer Country | SW |
Single Use | 3 |
Previous Use Code | 3 |
Event Type | 3 |
Type of Report | 3 |
Brand Name | ARTELON CMC SPACER |
Generic Name | SPACER |
Product Code | KYI |
Date Received | 2013-05-06 |
Operator | HEALTH PROFESSIONAL |
Device Availability | Y |
Device Age | DA |
Device Eval'ed by Mfgr | N |
Device Sequence No | 1 |
Device Event Key | 0 |
Manufacturer | ARTIMPLANT AB |
Manufacturer Address | HULDA MELLGRENS GATA 5 V. FROLUNDA SW |
Patient Number | Treatment | Outcome | Date |
---|---|---|---|
1 | 0 | 1. Other | 2013-05-06 |