FDA 510(k) Applications Submitted by Kapp Surgical Instrument, Inc.
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K030237 |
01/23/2003 |
KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT |
KAPP SURGICAL INSTRUMENT, INC. |
K050384 |
02/15/2005 |
KAPP BARI-RING, MODEL KS-BR-2005 |
KAPP SURGICAL INSTRUMENT, INC. |
K050655 |
03/14/2005 |
MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005 |
KAPP SURGICAL INSTRUMENT, INC. |
K050657 |
03/14/2005 |
MONDEAL CONTOUR HO SYSTEM |
KAPP SURGICAL INSTRUMENT, INC. |
K033930 |
12/18/2003 |
KAPP CUSTOM ULNAR HEAD WRIST IMPLANT |
KAPP SURGICAL INSTRUMENT, INC. |
K072216 |
08/09/2007 |
KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536 |
KAPP SURGICAL INSTRUMENT, INC. |
K200289 |
02/05/2020 |
Michler-Kapp Cardiovascular Vent Catheter |
Kapp Surgical Instrument, Inc. |
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