Depuy

  • Model / Serial
    Lot 2203528.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide.
  • Product Description
    Depuy PFC Oval Dome Patella (Part Number 960100)3-Peg, 32 mm, sterile; REF 96-0100.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Depuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
  • Source
    USFDA

318 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model Catalog: 5461-12-000 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 5461-10-000 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 5461-01-000 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 5460-14-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-16-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-18-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-20-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-22-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-10-000 (Lot serial: >1000 NUMBERS CONTACT MFR); Model Catalog: 5460-12-000 (Lot serial: >1000 NUMBERS CONTACT MFR)
  • Product Description
    DEPUY CEMENT RESTRICTOR (UNIVERSAL)
  • Manufacturer
  • Model / Serial
    All lots.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide Distribution.
  • Product Description
    Depuy DELTA Xtend, Standard Humeral PE Cup, Dia 42+6R RET, sterile, Depuy France; REF 130742106. || The device is used as a shoulder implant.
  • Manufacturer
  • Model / Serial
    All lots.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide Distribution.
  • Product Description
    DePuy DNP Anatomic Fracture Repair System, DNP Anatomic Right, Depuy, Warsaw, IN; REF DNPAR. || The device is used in the treatment of fractures and osteotomies of the distal radius.
  • Manufacturer
  • Model / Serial
    Product Code: 2894-10-300; Lot Number: 1208NT.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide Distribution -- Including states of MD, PA, NC, MO, NV, AZ, WI and CT.
  • Product Description
    DePuy Spine Expedium SFX Cross Connector System Torque Driver Shaft, Non-Sterile, REF: 2894-10-300. || Intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of acute and chronic instabilities or deformities of the spine.
  • Manufacturer
  • Model / Serial
    Lot Numbers: 2833275, 2833276, 2833277, 2833278, 2833279, 2835157, 2835908, 2835909, 2837020, 2838165, 2839666, 2839667, 2839668, 2839670, 2839671, 2839672, 2839675, 2840479, 2840480, 2841253, 2842526, 2842527, 2842528, 2842930, 2843263, 2843265, 2843267, 2843268, 2843270, 2844381, 2844383, 2844386, 2844796, 2844799, 2844800, 2845530, 2845534, 2846326, 2846330, 2846332, 2852392, 2852394, 2855015, 2855016, 2857271, 2857272, 2857881, 2857882, 2857884, 2857885, 2858572, 2858573, 2858574, 2858576, 2858577, 2859195, 2859197, 2859198, 2859199, 2859915, 2859916, 2859917, 2859920, 2860448, 2860449, 2860452, 2860455, 2860456, 2861519, 2861520, 2861699, 2862589, 2862591, 2863841, 2863843, 2864833, 2864834, 2864835, 2864837, 2864839, 2866038, 2868313, 2868314, 2869119, 2869120, 2869121, 2869122, 2869123, 2871182, 2871183, 2871835, 2871836, 2874434, 2874435, 2874436, 2876307, 2876309, 2876311, 2876314, 2881638, 2885685, 2885689, 2886278, 2886968 and 2886974.
  • Product Classification
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    Nationwide.
  • Product Description
    DePuy P.F.C. Sigma Knee System, Non-Porous Cruciate Retaining Femoral Component, 73 mm M/L 69 mm A/P, 5 left, sterile, DePuy Orthopaedics, Inc., Warsaw, IN; REF 96-0005. || The device is used for total or unicompartmental knee arthroplasty and is intended to provide increased patient mobility and reduced pain by replacing the damaged knee joint articulation in patients where there is evidence of sufficient sound bone to seat and support the components.
  • Manufacturer
313 more