FDA 510(k) Applications Submitted by ISOTIS ORTHOBIOLOGICS, INC
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K091193 |
04/23/2009 |
ACCELL EVO3C |
ISOTIS ORTHOBIOLOGICS, INC |
| K040419 |
02/18/2004 |
DYNAGRAFT II |
ISOTIS ORTHOBIOLOGICS, INC |
| K081817 |
06/26/2008 |
ACCELL TBM-R |
ISOTIS ORTHOBIOLOGICS, INC |
| K070751 |
03/19/2007 |
ORTHOBLAST II DBM DEMINERALIZED BONE MATRIX PASTE AND PUTTY |
ISOTIS ORTHOBIOLOGICS, INC |
| K050642 |
03/11/2005 |
ORTHOBLAST II PUTTY AND PASTE |
ISOTIS ORTHOBIOLOGICS, INC |
| K050690 |
03/17/2005 |
CONNEXUS |
ISOTIS ORTHOBIOLOGICS, INC |
| K041991 |
07/23/2004 |
ASPIREX - BONE MARROW ASPIRATE KIT |
ISOTIS ORTHOBIOLOGICS, INC |
| K052098 |
08/03/2005 |
CONNEXUS, .5CC, MODEL 023000-005 |
ISOTIS ORTHOBIOLOGICS, INC |
| K042706 |
09/30/2004 |
OSSATURA DENTAL |
ISOTIS ORTHOBIOLOGICS, INC |
| K043573 |
12/27/2004 |
DYNAGRAFT II DENTAL |
ISOTIS ORTHOBIOLOGICS, INC |
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