Kapp Surgical Instrument, Inc.
Kapp Surgical Instrument, Inc. holds FDA 510(k) medical device clearances, first cleared 1984, most recent 2021.
Top product codes for Kapp Surgical Instrument, Inc.
Recent clearances by Kapp Surgical Instrument, Inc.
- K200289 — Michler-Kapp Cardiovascular Vent Catheter
- K072216 — KAPP BARI-RING ENDOSCOPIC MARKER, MODEL K-9536
- K050384 — KAPP BARI-RING, MODEL KS-BR-2005
- K050655 — MONDEAL RADIUS HO SYSTEM, MODEL KS-MR-2005
- K050657 — MONDEAL CONTOUR HO SYSTEM
- K033930 — KAPP CUSTOM ULNAR HEAD WRIST IMPLANT
- K030237 — KAPP CUSTOM RADIAL HEAD ELBOW IMPLANT
- K844177 — COSGROVE MITRAL VALVE RETRACTOR
- K843368 — KAPP SPINAL BUTTON
Data sourced from openFDA. This site is unofficial and independent of the FDA.