MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed with the FDA on 2017-05-15 for VIPER 2 SCREW manufactured by Depuy Synthes Spine.
        [75209113]
This complaint was generated from literature review for health authority reporting purposes. The complaint product is not available for the investigation. A supplemental report is not anticipated unless the results of the pms identify a corrective action or additional relevant information. Should the product become available, a physical evaluation will be conducted and a supplemental report filed with the results. If information is obtained that was not available for the initial medwatch, a follow-up medwatch will be filed as appropriate.
 Patient Sequence No: 1, Text Type: N, H10
        [75209114]
This report is being filed after the subsequent review of the following literature article: wang, q. Y. , huang, m. G. , ou, d. Q. , xu, y. C. , dong, j. W. , yin, h. D. ,... & rong, l. M. (2017). One-stage extreme lateral interbody fusion and percutaneous pedicle screw fixation in lumbar spine tuberculosis. Journal of musculoskeletal & neuronal interactions, 17(1), 450. N= 1 post-op loosening.
 Patient Sequence No: 1, Text Type: D, B5
| Report Number | 1526439-2017-10363 | 
| MDR Report Key | 6568272 | 
| Date Received | 2017-05-15 | 
| Date of Report | 2017-04-18 | 
| Date Mfgr Received | 2017-04-18 | 
| Date Added to Maude | 2017-05-15 | 
| 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 | JASON BUSCH | 
| Manufacturer Street | 325 PARAMOUNT DRIVE | 
| Manufacturer City | RAYNHAM MA 02767 | 
| Manufacturer Country | US | 
| Manufacturer Postal | 02767 | 
| Manufacturer Phone | 5088808201 | 
| Manufacturer G1 | DEPUY SYNTHES SPINE | 
| Manufacturer Street | 325 PARAMOUNT DRIVE | 
| Manufacturer City | RAYNHAM MA 02767 | 
| Manufacturer Country | US | 
| Manufacturer Postal Code | 02767 | 
| Single Use | 3 | 
| Previous Use Code | 3 | 
| Event Type | 3 | 
| Type of Report | 0 | 
| Brand Name | VIPER 2 SCREW | 
| Generic Name | UNKNOWN VIPER SCREW | 
| Product Code | MRW | 
| Date Received | 2017-05-15 | 
| Device Availability | N | 
| Device Eval'ed by Mfgr | R | 
| Device Sequence No | 1 | 
| Device Event Key | 0 | 
| Manufacturer | DEPUY SYNTHES SPINE | 
| Manufacturer Address | 325 PARAMOUNT DRIVE RAYNHAM MA 02767 US 02767 | 
| Patient Number | Treatment | Outcome | Date | 
|---|---|---|---|
| 1 | 0 | 1. Other; 2. Required No Informationntervention | 2017-05-15 |