Smith and Nephew Donjoy, Inc.
FDA 510(k) medical device clearances.
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.