Synthes Spine Co.Lp
Synthes Spine Co.Lp holds FDA 510(k) medical device clearances, first cleared 2005, most recent 2012.
Top product codes for Synthes Spine Co.Lp
Recent clearances by Synthes Spine Co.Lp
- K121852 — SYNTHES ZERO-P VARIABLE ANGLE (VA)
- K112459 — SYNTHES ZERO-P
- K112068 — SYNTHES ZERO-P VARIABLE ANGLE (VA)
- K103320 — SYNTHES XRL
- K081568 — ANTEGRA-T
- K080020 — ARCOFIX
- K072981 — SYNTHES ZERO-P
- K072434 — SYNTHES OC FUSION AND SYNAPSE SYSTEMS
- K072253 — SYNFIX-LR SPACER
- K070573 — SYNAPSE SYSTEM
- K062083 — SYNFIX -LR
- K062933 — SYNTHES ORACLE SPACER
- K063158 — SYNTHES ANTEGRA SYSTEM
- K053418 — SYNTHES OC FUSION SYSTEM
- K061891 — SYNEX II
- K053508 — SYNFIX-LR
- K052151 — SYNTHES PANGEA MONOAXIAL SYSTEM
- K050451 — SYNTHES VECTRA SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.