FDA Adverse Event Injury Summary report: N

TSRH SPINAL SYSTEM

MDR report key: 6978960 · Received October 26, 2017

Report

Report Number
1030489-2017-02250
Event Type
Injury
Date Received
October 26, 2017
Date of Event
September 27, 2017
Report Date
November 7, 2017
Manufacturer
WARSAW ORTHOPEDICS
Product Code
NKB
PMA / PMN Number
SEE H10
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
JA
Reporter Occupation
PHYSICIAN

Narratives

Additional Manufacturer Narrative · 1

ALTHOUGH IT IS UNKNOWN WHICH OF THE DEVICES LED TO THE EVENT, HOWEVER, WE ARE FILING THIS REPORT FOR NOTIFICATION PURPOSES. FOLLOWING DEVICES WERE INVOLVED: PART# LOT# QTY SIMILAR DEVICE 510K# UPN 0350269W, 1, 83565459, K090740, (B)(4), GX83565459; 490544W, 2, 83565459, K090740, (B)(4), GX83565459; 0361972W, 1, 83565459, K090740, (B)(4). IF INFORMATION IS PROVIDED IN THE FUTURE, A SUPPLEMENTAL REPORT WILL BE ISSUED.

Additional Manufacturer Narrative · 1

THIS PART IS NOT APPROVED FOR USE IN THE US, HOWEVER A LIKE DEVICE WITH PART# (B)(4), 510K# K090740 AND UPN (B)(4) IS APPROVED FOR SALE. NEITHER THE DEVICE NOR FILMS OF APPLICABLE IMAGING STUDIES WERE RETURNED TO THE MANUFACTURER FOR EVALUATION. THEREFORE, WE ARE UNABLE TO DETERMINE THE DEFINITIVE CAUSE OF THE REPORTED EVENT.

Description of Event or Problem · 1

PRE-OP DIAGNOSIS: L4 BURST FRACTURE PROCEDURE: L4: VERTEBROPLASTY; L3-5: POSTERIOR FUSION IT WAS REPORTED THAT POST-OP, CT EXAM REVEALED SCREW MALPOSITION AT L5. PATIENT SUFFERED WITH LOW BACK PAIN, LOWER EXTREMITY PAIN AND MUSCLE WEAKNESS AS A RESULT AND UNDERWENT A REVISION ON (B)(6) 2017 TO ADJUST THE POSITIONS OF THE SCREWS.

Devices

Seq Brand Generic Product Code Manufacturer Model Lot UDI-DI
761271 TSRH SPINAL SYSTEM ORTHOSIS, SPINAL PEDICLE FIXATION, FOR DEGENERATIVE DISC DISEASE NKB WARSAW ORTHOPEDICS NA UNK

Patients

Seq Age Sex Outcome Treatment
1 80 YR Other| R