COMP LK SCR 3.5HEX 4.75X20 ST N/A 180551

MAUDE Adverse Event Report

MAUDE data represents reports of adverse events involving medical devices. This maude entry was filed from a company representative,health report with the FDA on 2020-03-16 for COMP LK SCR 3.5HEX 4.75X20 ST N/A 180551 manufactured by Zimmer Biomet, Inc..

MAUDE Entry Details

• Report Number: 0001825034-2020-01108
• MDR Report Key: 9835912
• Report Source: COMPANY REPRESENTATIVE,HEALTH
• Date Received: 2020-03-16
• Date of Report: 2020-03-25
• Date Mfgr Received: 2020-03-24
• Device Manufacturer Date: 2019-03-21
• Date Added to Maude: 2020-03-16
• 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: MS. CHRISTINA ARNT
• Manufacturer Street: 56 E. BELL DR.
• Manufacturer City: WARSAW IN 46582
• Manufacturer Country: US
• Manufacturer Postal: 46582
• Manufacturer Phone: 5745273773
• Manufacturer G1: ZIMMER BIOMET, INC.
• Manufacturer Street: 56 E. BELL DRIVE
• Manufacturer City: WARSAW IN 46582
• Manufacturer Country: US
• Manufacturer Postal Code: 46582
• Single Use: 3
• Previous Use Code: 3
• Removal Correction Number: N/A
• Event Type: 3
• Type of Report: 3

Device Details

• Brand Name: COMP LK SCR 3.5HEX 4.75X20 ST
• Generic Name: FASTENER, FIXATION
• Product Code: KWS
• Date Received: 2020-03-16
• Model Number: N/A
• Catalog Number: 180551
• Lot Number: 139860
• Operator: HEALTH PROFESSIONAL
• Device Availability: N
• Device Age: DA
• Device Eval'ed by Mfgr: R
• Device Sequence No: 1
• Device Event Key: 0
• Manufacturer: ZIMMER BIOMET, INC.
• Manufacturer Address: 56 E. BELL DRIVE WARSAW IN 46582 US 46582

Patients

Patient Number	Treatment	Outcome	Date
1	0	1. Hospitalization; 2. Required No Informationntervention	2020-03-16