FDA 510(k) Applications Submitted by CARRIE HARTILL

FDA 510(k) Number Submission Date Device Name Applicant
K050767 03/25/2005 STERLING INTERFERENCE SCREW ST REGENERATION TECHNOLOGIES, INC.
K051615 06/17/2005 STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES REGENERATION TECHNOLOGIES, INC.
K052405 09/01/2005 STERLING INTERFERENC SCREW HT REGENERATION TECHNOLOGIES, INC.
K043420 12/13/2004 OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE REGENERATION TECHNOLOGIES, INC.
K043421 12/13/2004 OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC REGENERATION TECHNOLOGIES, INC.


Search | Companies | Product Codes | Device Names | Contacts | Applications | Decisions | Contact