25 results · 21ms · Sources: EU EUDAMED, US FDA

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FOUNDATION POROUS HIP STEM

FDA 510(k)
FDA Class 2 ·Orthopedic

CAPSTONE® Spinal System

FDA UDI
MEDTRONIC SOFAMOR DANEK, INC.·00613994290953·SPACER 2991226 CAPSTONE PEEK 12X26

Monolith

FDA UDI
Nuvasive, Inc.·00887517697837·Monolith Core, Ø12x26mm

Pro-Retractor Malleable Blade

FDA UDI
KOROS U.S.A., INC.·10840199542540·Pro-Retractor Malleable Blade Medium 2 x 6"

PLATELET-CHEX PLUS

FDA 510(k)
FDA Class 2 ·Hematology

Arthrex SwiveLock Suture Anchor

FDA 510(k)
FDA Class 2 ·Orthopedic

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·WARSAW ORTHOPEDIC INC.·Product code MAX·December 21, 2009

CATGUT CHROMIC 2/0 (3.5) 100M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL SA·Product code GAL·November 27, 2018

CATGUT CHROMIC 3 (7) 50M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL SA·Product code GAL·November 20, 2018

APPLIANCE, FIXATION, SPINAL INTERLAMINAL

FDA Adverse Event
Injury ·MEDTRONIC SOFAMOR DANEK·Product code KWP·September 29, 2017

ACCU-CHEK ® AVIVA PLUS TEST STRIPS

FDA Adverse Event
Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·March 6, 2013

MAXIMO II DR

FDA Adverse Event
Injury ·MEDTRONIC MED REL, INC.·Product code LWS·February 15, 2011

SPRINT FIDELIS

FDA Adverse Event
Injury ·MPRI·Product code LWS·August 8, 2014

CAPSTONE SPINAL SYSTEM

FDA Adverse Event
Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code MAX·March 15, 2016

CATGUT PLAIN 3/0 (3) 100M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAL·May 28, 2020

CATGUT PLAIN 1 (5) 75M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAL·July 20, 2020

CATGUT PLAIN 1 (5) 75M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAL·February 10, 2021

CATGUT CHROMIC 2 (6) 50M

FDA Adverse Event
Malfunction ·B. BRAUN SURGICAL, S.A.·Product code GAL·February 25, 2021

MEDIUM CHROM CAT 3/0 (3) 100M BAYER EE

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAL·February 17, 2020

CATGUT PLAIN 6 (10) 25M D2

FDA Adverse Event
Malfunction ·B.BRAUN SURGICAL SA·Product code GAL·December 31, 2019