Device Recall Advanced Orthogonal Percussion Adjusting Instrument

  • Modèle / numéro de série
    Serial numbers: 001, 002, 008, 007, 006, 0010, 009, 011, 016, 015, 014, 023, 017, 018, 019, 020, 021, 024, 025, 022, 027, 026, 028, 029, 030, 031, 032, 033, 034, 035, 036, 038, 039, 037, 041, 042, 040, 043, 044, 045, 046, 048, 049, 050, 052, 053, 055, 056, 060, 058, 059, and 061
  • Classification du dispositif
  • Classe de dispositif
    Unclassified
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide distribution: US including states of: AL, CA, CO, FL, GA, ID, KY, MD, NC, NJ, NY, OH, PA, TN, VA, and WA.
  • Description du dispositif
    Advanced Orthogonal Percussion Adjusting Instrument || Indicated for use by a licensed Chiropractor to assist in making Chiropractic adjustments to the Atlas vertebra.
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Advanced Orthogonal Equipment, Incorporated, 2201 62nd Ave N, Saint Petersburg FL 33702-5660
  • Source
    USFDA