Turnkey Intergration USA, Inc.
FDA 510(k) medical device clearances.
Top product codes for Turnkey Intergration USA, Inc.
Recent clearances by Turnkey Intergration USA, Inc.
- K991405 — OMNI-FIX, HUMERAL NAIL
- K990523 — B2C, ESPACE REVISION CUP SYSTEM
- K990307 — OMNI-FIX, NAIL SYSTEM
- K972411 — LINK CEMENT PLUG
- K970284 — ARTOS, DIPLOS SYSTEM
- K970084 — LINK CERCLAGE WIRE SYSTEM
- K953653 — LUBINUS SP II HIP SYSTEM
- K943986 — LINK ENDO MODEL REVISION CUP
- K951355 — LINK SADDLE PROTHESIS
- K950397 — SYSTEM 22 VALVE
- K940297 — UNIVERSAL WRIST
- K943277 — LINK SADDLE PROTHESIS
- K931960 — NUFFIELD TOTAL KNEE
- K923911 — INTRINSIC STEM
- K923898 — C-FIT CEMENTED HIP STEM
- K913708 — VENUS HIP
- K912985 — LIMA 28MM CERAMIC HEAD, MODIFICATION
- K913282 — LIMA RPS SHOULDER
- K912936 — MAY HUMERUS PLATES
- K911338 — LIMA CEMENT RESTRICTOR
- K910547 — FELDMUEHLE CERAMIC HEAD (12/14 X 28MM)
- K910548 — FELDMUEHLE CERAMIC HEAD (12/14 X 32MM)
- K910010 — Q SYSTEM 28 HIP STEM
- K903957 — VSP HIP STEM
- K902110 — MODIFIED FREEMAN ACETABULAR CUP
- K902111 — MODIFIED FREEMAN REVISION ACETABULAR CUP
Data sourced from openFDA. This site is unofficial and independent of the FDA.