Device Recall RESTORIS MCK TIBIAL BASEPLATE

  • Model / Serial
    Size 2 Item # 180612 Lot # 26080317-01 and  Size 7 Item # 180617 Lot # 26150217-01.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    AL, AR, AZ, CA, CO, FL, GA, ID, IL, IN, KS, LA, MA, MD, MI, MN, NC, NE, NH, NJ, NY, OK, OR, PA, RI, SC, TX, UT, VA, WA, WY, and Hawaii Australia, Italy, Netherlands, Singapore, South Korea, United Kingdom, and Vietnam
  • Product Description
    RESTORIS MCK TIBIAL BASEPLATE-RM/LL used in unicompartmental knee arthroplasty and knee replacements.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Mako Surgical Corporation, 2555 Davie Rd Ste 110, Davie FL 33317-7424
  • Source
    USFDA