Avanta Orthopaedics, Inc.
Avanta Orthopaedics, Inc. holds FDA 510(k) medical device clearances, first cleared 1997, most recent 2003.
Top product codes for Avanta Orthopaedics, Inc.
Recent clearances by Avanta Orthopaedics, Inc.
- K030881 — AVANTA CARPAL FUSION PLATING SYSTEM
- K021859 — WRIST IMPLANT
- K023604 — MODIFICATION TO RADIAL HEAD IMPLANT
- K013629 — FINGER JOINT PROSTHESIS
- K010847 — K'FIX
- K011819 — RADIAL HEAD IMPLANT
- K003033 — SCAPHIX, STAPLE, FIXATION, BONE
- K010786 — ULNAR HEAD IMPLANT
- K002644 — RADIAL HEAD IMPLANT
- K990596 — DISTAL RADIUS FRACTURE FIXATION PLATE SYSTEM
- K982268 — ULNAR HEAD IMPLANT
- K982288 — RADIAL HEAD IMPLANT
- K981715 — DISTAL RADIUS FRACTURE FIXATION PLATE
- K981716 — EXTERNAL FIXATION
- K974911 — EXTERNAL FIXATOR
- K965204 — AVANTA ORTHOPAEDICS TRAPEZIUM IMPLANT
- K964359 — AVANTA ORTHOPAEDICS TENDON SPACER
- K964381 — AVANTA ORTHOPAEDICS TRAPEZIAL IMPLANT
Data sourced from openFDA. This site is unofficial and independent of the FDA.