FDA 510(k) Applications Submitted by REGENERATION TECHNOLOGIES, INC.
| 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. |
| K060180 |
01/23/2006 |
BIOSET XC |
REGENERATION TECHNOLOGIES, INC. |
| K060253 |
02/01/2006 |
STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST. |
REGENERATION TECHNOLOGIES, INC. |
| K072327 |
08/20/2007 |
CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON |
REGENERATION TECHNOLOGIES, INC. |
| K063584 |
12/01/2006 |
STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937 |
REGENERATION TECHNOLOGIES, INC. |
| K080418 |
02/15/2008 |
REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PAST |
REGENERATION TECHNOLOGIES, INC. |
| K072238 |
08/13/2007 |
BIOSET XCH |
REGENERATION TECHNOLOGIES, INC. |
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