InjuryKWD
CARTIVA
Received May 28, 2019 · Event occurred Dec 8, 2017
Report MW5086955 · MDR key 8650579
Device
Generic name
Prosthesis, Toe, Hemi, Phalangeal
Manufacturer
Cartiva, Inc.Product problems
- Break
Patient
60 YR
- Pain
- Pain
Narrative
Description of Event or Problem
REVISION OF DAMAGED/SUBSIDED IMPLANT WITH CONTINUED PAIN. FDA SAFETY REPORT ID # (B)(4).