MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,foreig report with the FDA on 2019-05-23 for UNK - PLATES: MATRIX ORBITAL manufactured by Oberdorf Synthes Produktions Gmbh.
[145984964]
Brand name, common device name, procode, mfr, lot #, part #, udi #, 510k: this report is for an unknown synthes titanium mesh implant/unknown lot. Part and lot numbers are unknown; udi number is unknown. Device evaluated by mfr, manufacture date: without a lot number the device history records review could not be completed. Product was not returned. Based on the information available, it has been determined that no corrective and/or preventative action is proposed. This complaint will be accounted for and monitored via post market surveillance activities. If additional information is made available, the investigation will be updated as applicable. Device was used for treatment, not diagnosis. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate. (b)(4).
Patient Sequence No: 1, Text Type: N, H10
[145984965]
This report is being filed after the review of the following journal article: pedemonte, c. Et al. (2018), reconstruction of medial orbital wall using a retrocaruncular approach, journal of cranio-maxillo-facial surgery, vol. 46, pages 1726-1730 (chile). The purpose of this study is to analyze and describe the use of the retrocaruncular approach for the treatment of medial orbital wall fractures. During january 2011 and january 2017, a total of 30 patients underwent orbital reconstruction treatment with a retrocaruncular approach together with a transconjunctival extension and lateral canthotomy using an unknown synthes titanium mesh implant (matrixorbital). The minimum follow-up was 6 months. The following complications were reported as follows: 1 patient presented a delayed complication on the 5th day after the operation, developing a conjunctival granuloma on the caruncle of the affected eye socket. The granuloma was associated with a stitch to the inferior oblique muscle and was removed in an exploratory surgery without need to remove the mesh to resolve it. 1 patient developed delayed enophthalmos of the eye socket that was operated on after the 1st surgery, making a 2nd surgical intervention necessary to restore the lost orbital volume using customized implants. 1 patient, though unrelated to the type of approach used, developed post-traumatic glaucoma after 2 months. This is for an unknown synthes titanium mesh implant (matrixorbital). This is report 1 of 2 for (b)(4).
Patient Sequence No: 1, Text Type: D, B5
| Report Number | 8030965-2019-64435 |
| MDR Report Key | 8636822 |
| Report Source | COMPANY REPRESENTATIVE,FOREIG |
| Date Received | 2019-05-23 |
| Date of Report | 2019-04-24 |
| Date Mfgr Received | 2019-06-21 |
| Date Added to Maude | 2019-05-23 |
| 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 |
| Reporter Occupation | OTHER HEALTH CARE PROFESSIONAL |
| Health Professional | 3 |
| Initial Report to FDA | 3 |
| Report to FDA | 3 |
| Event Location | 3 |
| Manufacturer Contact | KARA DITTY-BOVARD |
| Manufacturer Street | 1302 WRIGHTS LANE EAST |
| Manufacturer City | WEST CHESTER PA 19380 |
| Manufacturer Country | US |
| Manufacturer Postal | 19380 |
| Manufacturer Phone | 6103142063 |
| Single Use | 3 |
| Previous Use Code | 3 |
| Event Type | 3 |
| Type of Report | 3 |
| Generic Name | IMPLANT, ORBITAL, EXTRA-OCULAR |
| Product Code | HQX |
| Date Received | 2019-05-23 |
| Catalog Number | UNK - PLATES: MATRIX ORBITAL |
| Operator | HEALTH PROFESSIONAL |
| Device Availability | N |
| Device Age | DA |
| Device Eval'ed by Mfgr | R |
| Device Sequence No | 1 |
| Device Event Key | 0 |
| Manufacturer | OBERDORF SYNTHES PRODUKTIONS GMBH |
| Manufacturer Address | EIMATTSTRASSE 3 OBERDORF 4436 SZ 4436 |
| Patient Number | Treatment | Outcome | Date |
|---|---|---|---|
| 1 | 0 | 1. Required No Informationntervention | 2019-05-23 |