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. |
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