Device Recall Drill guide for the JAWS Nitinol Staple System

  • Model / Serial
    Part # P71-008-0808-S 8mm x 8mm x 8mm, Straight Lots 260315217A, 260322017A, 260326217A and 260326217B., Part # P71-010-1010-S 10mm x 10mm x 10mm, Straight Lots 260317717A, 260317717C, 260322017B, and 260326217D., Part # P71-108-0808-S 8mm x 8mm x 8mm, Angled, Lots 260322017C, 260322017D, 260315217B, and 260326217M. and  Part # P71-110-1010-S 10mm x 10mm x 10mm, Angled Lots 260326217E,  260317717B, 260322017E, 260322017F, 260322017G, 260326217F and 260326217G.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Worldwide Distribution: US (nationwide) to states of: AL, AZ, CA, CO, DC, FL, GA, ID, IL, IN, KS, KY, LA, MD, ME, MI, MN, MO, NC, NJ, NV, NY, OH, OR, PA, SC, TN, TX, VA, WA, and WI; to countries of: Australia and South Africa.
  • Product Description
    P28 JAWS Nitinol Staple System kits are designed for use in an osteotomy, arthrodesis and fragment fixation of bones and joints of the foot including fixation of small bone fragments.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Paragon 28, Inc., 4B Inverness Ct E Ste 280, Englewood CO 80112-5329
  • Manufacturer Parent Company (2017)
  • Source
    USFDA