Interarticular Disc Prosthesis (interpositional Implant)

Device Code: 1324

Product Code(s): MPJ

Device Classification Information

• Device Type ID: 1324
• Device Name: Interarticular Disc Prosthesis (interpositional Implant)
• Regulation Description: Interarticular Disc Prosthesis (interpositional Implant).
• Regulation Medical Specialty: Dental
• Review Panel: Dental
• Premarket Review: Office Of Device Evaluation (ODE); Division Of Anesthesiology, General Hospital, Infection Control, And Dental Devices (DAGRID); Dental Devices Branch (DEDB)
• Submission Type: PMA
• CFR Regulation Number: 872.3970 [🔎]
• FDA Device Classification: Class 3 Medical Device
• Product Code: MPJ
• GMP Exempt: No
• Summary MR: Eligible
• Implanted Device: Yes
• Life Support Device: No
• Third Party Review: Not Third Party Eligible

Recognized Standards

• 4-212 ISO 7405 Second Edition 2008-12-15
  Dentistry - Evaluation Of Biocompatibility Of Medical Devices Used In Dentistry [Including: Amendment 1 (2013)]

Total Product Life Cycle

• Device Type ID: 1324
• Device: Interarticular Disc Prosthesis (interpositional Implant)
• Product Code: MPJ
• FDA Device Classification: Class 3 Medical Device
• Regulation Description: Interarticular Disc Prosthesis (interpositional Implant).
• CFR Regulation Number: 872.3970 [🔎]

TPLC Last Update: 2019-04-02 19:52:02