Synthes (Usa)
FDA 510(k) medical device clearances.
Clearances by Synthes (Usa) — page 5
401–411 of 411- K904553 — BONE STAPLE(S)
- K894098 — SYNTHES EXTERNAL FIXATION BONE CLIP
- K884688 — MODULAR SPINAL FIXATION & LOCKING HOOK SPINAL ROD
- K840955 — CONDYLAR PROSTHESIS OF MANDIBLE W/HEAD
- K840954 — DYNAMIC CONDYLAR SCREW OR D.C.S.
- K823495 — MOBILIMB-CPM UPPER/LOWER LIMB DEVICE
- K802462 — SYNTHES SPINAL IMPLANT SYSTEM
- K792291 — SYNTHES RECONSTRUCTIVE PLATES 'Y' PLATES
- K792253 — ARICULATED TENSION DEVICE SYNTHES TEN
- K791619 — DYNAMIC HIP SCREW
- K770405 — OVERLOAD WARNING DEVICE
Data sourced from openFDA. This site is unofficial and independent of the FDA.