Smith & Nephew, Inc., Orthopaedic Div.
Smith & Nephew, Inc., Orthopaedic Div. holds FDA 510(k) medical device clearances, first cleared 1996, most recent 1999.
Top product codes for Smith & Nephew, Inc., Orthopaedic Div.
Recent clearances by Smith & Nephew, Inc., Orthopaedic Div.
- K991538 — OPERA CUPFLANGED ACETABULAR COMPONENTS
- K970635 — TITANIUM SPINAL ROD SYSTEM
- K971414 — ZIRCONIA PROZYR CERAMIC 12/14 GLOBAL TAPER (GT) FEMORAL HEADS
- K970748 — TAYLOR SPATIAL FRAME EXTERNAL FIXATION SYSTEM
- K970751 — HEIDELBERG EXTERNAL FIXATOR
- K970713 — COMPASS UNIVERSAL HINGE
- K970337 — HA GLOBAL TAPER (GT) TAPERED HIP STEM
- K970351 — GLOBAL TAPER SPECTRON HIP STEMS
- K963255 — PROFIX PLUS TIBIAL INSERT, PROFIX PS PLUS TIBIAL INSERT, PROFIX P/S TIBIAL INSERT
- K962784 — ULTIUM SPINAL PLATING SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.