HOOK, BONE
FDA product code KIK · Class 1 · 3 devices · 6 reports · 0 devices named in recalls
- MORELAND 2422-03-000Depuy Orthopaedics, Inc. · HOOK, BONE3 reports
- NA 6020-13-000Depuy (Ireland) · HOOK, BONE2 reports
- V. Mueller OS4080-002Steris Corporation · HOOK, BONE1 report