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Regeneration Technologies, Inc.

FDA 510(k) & PMA Approved Devices — 11 products

Total Devices11
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K080418 REGENAFIL, REGENAFORM, ALRIVA DBM PASTE, SLTIVA DM WITH CORTICAL CANCELLOUS SHIPS, BIOSET, SIOSET IC, RTI ALLOGRAFT PASTNUN2008-04-30 View
510(k) K072238 BIOSET XCHMQV2008-01-25 View
510(k) K072327 CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTONMQV2007-10-24 View
510(k) K063584 STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID3937HWC2007-05-09 View
510(k) K060180 BIOSET XCMBP2006-09-06 View
510(k) K060253 STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST.HWC2006-02-23 View
510(k) K052405 STERLING INTERFERENC SCREW HTHWC2005-11-16 View
510(k) K051615 STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBESMQV2005-08-15 View
510(k) K050767 STERLING INTERFERENCE SCREW STHWC2005-06-09 View
510(k) K043421 OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP ICMQV2005-02-16 View
510(k) K043420 OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTEMQV2005-02-10 View
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