Product code MJT— Unknown
BIPOLAR SHOULDER PROSTHESIS-SHELL(RD-113130/33, BIANGULAR MODULAR HEAD(RD-113101/41/42,BIOMODULAR MODULAR HEAD(RD-113143
- Classification name
- Prosthesis, Shoulder, Humeral (Bipolar Hemi-Shoulder) Metal/Polymer, Cemented Or Uncemented
- Device class
- Class 3
- Advisory panel
- Unknown
- Total cleared
- 3
- First cleared
- Most recent
Market context for product code MJT
FDA has cleared devices under product code MJT between 1997 and 1999, filed by 3 applicant companies. No FDA device recalls reference this product code. Class III devices are high-risk and generally require premarket approval (PMA); 510(k) clearance under a Class III product code is limited to certain preamendments-type devices.
Clearances per year
- 1999
- 1997
Top applicants under product code MJT
Recent clearances under product code MJT
Data sourced from openFDA. This site is unofficial and independent of the FDA.