FASTENER, PLATE, CRANIOPLASTY

FDA product code HBW · Class 2 · 16 devices · 79 reports · 1 devices named in recalls

• RapidSorb 530.553.01S

  Synthes GmbH · FASTENER, PLATE, CRANIOPLASTY
  1 recall0 reports
• "1.5MM" SYSTEM 95-6104

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  30 reports
• "1.5MM" SYSTEM 95-6105

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  16 reports
• UNIVERSAL NEURO 3 56-15904

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  7 reports
• 1.5MM SYSTEM 91-6104-50

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  6 reports
• 1.5MM SYSTEM 91-6105X

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  5 reports
• Universal Neuro 3 56-15934

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  4 reports
• Universal Neuro 3 56-15034

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  2 reports
• Universal Neuro 3 56-15935

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  2 reports
• 1MM SYSTEM 01-7404

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  1 report
• "1.5MM" SYSTEM 91-1805

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  1 report
• TMS SYSTEM 25-2307

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  1 report
• 1.5MM SYSTEM 01-8679

  Biomet Microfixation, Inc · FASTENER, PLATE, CRANIOPLASTY
  1 report
• RESORB XG, STERILE 52-808-13-04

  KLS-Martin L.P. · FASTENER, PLATE, CRANIOPLASTY
  1 report
• NA 12-01542S

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  1 report
• Universal Neuro 3 56-15933

  Stryker Leibinger GmbH & Co. KG · FASTENER, PLATE, CRANIOPLASTY
  1 report