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Modified Instrument - HXX

FDA UDI
Ulrich Medical Usa, Inc.·00810076335070·Self-Retaining SR25 Screwdriver, 10" length

Reform Pedicle Screw System

FDA UDI
PRECISION SPINE, INC.·00840019928809·Driver with Mechanical Lock

Vault C ACDF System

FDA UDI
PRECISION SPINE, INC.·00840019917162·Screw Inserter

Intervertebral Body Fusion Device

FDA UDI
PRECISION SPINE, INC.·00840019922487·Straight Vault ALIF Screwdriver

HXX

FDA Adverse Event
Malfunction ·PRECISION SPINE, INC·Product code HXX·November 6, 2023

VENOUS RESERVOIR VRS-XXX SERIES; HOLDER VRS-HXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

CARDIOTOMY RESERVOIR BRS-XXX & HOLDER BRS-HXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

ARTERIAL FILTER AFS-XX /FILTER HOLDER AFS-HXX

FDA 510(k)
FDA Class 2 ·Cardiovascular

Slimplicity Anterior Cervical Plate System

FDA UDI
PRECISION SPINE, INC.·00840019931038·Slimplicity Driver, AO Connect, 6.4"

Slimplicity Anterior Cervical Plate System

FDA UDI
PRECISION SPINE, INC.·00840019931021·Slimplicity Driver, AO Connect, 5.5"

Howsport

FDA UDI
JIAXING HOW SPORT MEDICAL INSTRUMENT CO., LTD.·06975380614083·

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014

2.0MM CANNULATED DRILL BIT/QC 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWE·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/34MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/15MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/15MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW LONG THREAD/32MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code HWC·June 12, 2014

3.0MM TI CANNULATED SCREW SHORT THREAD/32MM

FDA Adverse Event
Malfunction ·SYNTHE USA·Product code HWC·June 12, 2014

1.1MM THREADED GUIDE WIRE 150MM

FDA Adverse Event
Malfunction ·SYNTHES USA·Product code FZX·June 12, 2014