Smith and Nephew Donjoy, Inc.
Smith and Nephew Donjoy, Inc. holds FDA 510(k) medical device clearances, first cleared 1991, most recent 1997.
Top product codes for Smith and Nephew Donjoy, Inc.
Recent clearances by Smith and Nephew Donjoy, Inc.
- K970051 — MUSCLESENSE II CLINICAL ELECTROMYOGRAPHY DEVICE
- K963489 — WHEEL CHAIR ACCESSORY
- K963490 — PROTECTIVE RESTRAINT - BELTS
- K963492 — PROTECTIVE RESTRAINT
- K962462 — MUSCLEMAX PLUS ELECTRICAL MUSCLE STIMULATOR
- K955057 — MODEL 1100 COLD THERAPY DEVICE
- K951350 — MUSCLESENSE ELECTROMYOGRAPHY DEVICE
- K945687 — ROUNDED CANNULATED INSIDE-OUT (RCI) ACL SCREW
- K946313 — TIBIAL ROUTERS, FEMORAL ROUTERS AND TUBE GRAFT SIZER
- K945236 — AIMS CANNULATED ACL SCREW (7MM DIAMETER)
- K932592 — BRACE NEUTRALIZER
- K932862 — ROUNDED CANNULATED INSIDE-OUT (RCI) ACL SCREW
- K934044 — ANTERIOR CRUCIATE LIGAMENT (ACL) SURGICAL INSTRUMENTATION SYSTEM
- K932320 — NEUTRALIZER
- K903823 — SPEEDWRAP, DYNAWRAP, DYNAPLAST TAPE
Data sourced from openFDA. This site is unofficial and independent of the FDA.