FDA 510(k) Applications Submitted by JOHN KAPITAN
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K070891 |
03/30/2007 |
ALTIVA CLASSIC ACP SYSTEM |
ALTIVA CORP. |
| K051216 |
05/12/2005 |
HYDRALOK SYSTEM |
ALTIVA CORP. |
| K061482 |
05/30/2006 |
ALTES BUTTRESS PLATING SYSTEM |
ALTIVA CORP. |
| K121672 |
06/06/2012 |
AFT PROXIMAL HUMERUS FRACTURE PLATE |
SHOULDER OPTIONS, INC. |
| K102539 |
09/03/2010 |
ICUFF REPAIR PLATE, RIGHT; CUFF REPAIR PLATE. LEFT; ANCHOR BOLT, 10MM THROUGH 50MM |
SHOULDER OPTIONS, INC. |
| K132925 |
09/18/2013 |
SAVANNAH-T, REDUCTION, SAVANNAH-T, HIGH-TOP, SAVANNAH-T, MONOAXIAL MID-TOP, SAVANNAH-T, LOW-TOP, SAVANNAH-LINK |
AMENDIA, INC. |
| K102957 |
10/05/2010 |
CUTTING EDGE SPINE INTERBODY FUSION DEVICE |
CUTTING EDGE SPINE, LLC |
| K133668 |
11/29/2013 |
AFT GREATER TUBEROSITY FRACTURE PLATE, LEFT, AFT GREATER TUBEROSITY FRACTURE PLATE, RIGHT, AFT GREATER TUBEROSITY CANNUL |
SHOULDER OPTIONS, INC. |
| K124014 |
12/27/2012 |
SUREFIX INTERSPINOUS FUSION SYSTEM |
JG SPINE, LLC |
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