Turnkey Intergration USA, Inc.
Turnkey Intergration USA, Inc. holds FDA 510(k) medical device clearances, first cleared 1990, most recent 1999.
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.