FDA Adverse Event Injury Summary report: N

PROSTHESIS INTERVERTEBRAL DISC

MDR report key: 4777872 · Received May 18, 2015

Report

Report Number
2530088-2015-10355
Event Type
Injury
Date Received
May 18, 2015
Report Date
April 28, 2015
Manufacturer
SYNTHES BRANDYWINE
Product Code
MJO
PMA / PMN Number
PP050010
Adverse Event
Yes
Report Source
Manufacturer report
Reporter Location
SZ
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

DEVICE USED FOR TREATMENT NOT DIAGNOSIS THIS REPORT IS FOR UNKNOWN PRODISC-L IMPLANT, PDL INFERIOR ENDPLATE . UDI # UNKNOWN PART AND LOT NUMBER, UDI IS UNAVAILABLE. (B)(6). INCREASED SEGMENTAL LORDOSIS AND ANTERIOR POSITIONING. THE INVESTIGATION COULD NOT BE COMPLETED AND NO CONCLUSION COULD BE DRAWN, AS NO DEVICE WAS RETURNED AND NO LOT NUMBER WAS PROVIDED. IF INFORMATION IS OBTAINED THAT WAS NOT AVAILABLE FOR THE INITIAL MEDWATCH, A FOLLOW-UP MEDWATCH WILL BE FILED AS APPROPRIATE.

Description of Event or Problem · 1

THIS REPORT IS BEING FILED AFTER THE SUBSEQUENT REVIEW OF THE FOLLOWING JOURNAL ARTICLE: LEE C, CHUNG S, OH S , YOU J. MAY 2011 SIGNIFICANCE OF ANGULAR MISMATCH BETWEEN VERTEBRAL ENDPLATE IN LUMBAR TOTAL DISC REPLACEMENT. J SPINAL DISORDER TECH, 24:183-188. (B)(4). FROM (B)(6) 2002 TO (B)(6) 2006 56 PATIENTS (33 FEMALES AND 23 MALES, AVERAGE AGE OF 44.7 YEARS) UNDERWENT TOTAL DISC REPLACEMENT WITH PRODISC-L THE MEAN FOLLOW UP PERIOD WAS 25.6 MONTHS. RADIOGRAPHIC EVALUATIONS AND VARIOUS OTHER ASSESSMENT TOOLS WERE UTILIZED AT ONE WEEK, 6 WEEKS, 6 MONTHS AND ONE YEAR AFTER OPERATION. COMPLICATIONS: 6 PATIENTS EXPERIENCED INCREASED SEGMENTAL LORDOSIS AND ANTERIOR POSITIONING; 6 PATIENTS EXPERIENCED A DECREASED RANGE OF MOTION. THIS REPORT 4 OF 6 FOR (B)(4). THIS REPORT IS FOR A PRODISC-L WITH AN UNKNOWN PART NUMBER, LOT NUMBER AND QUANTITY

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
322948 PROSTHESIS INTERVERTEBRAL DISC MJO SYNTHES BRANDYWINE

Patients

Seq Age Sex Outcome Treatment
1 Required Intervention