Synthes Spine Co.Lp
FDA 510(k) medical device clearances.
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.