Amedica Corp.
Amedica Corp. holds FDA 510(k) medical device clearances, first cleared 2002, most recent 2018.
Top product codes for Amedica Corp.
Recent clearances by Amedica Corp.
- K173453 — Valeo® C+CSC with Lumen Interbody Fusion Device
- K161405 — Valeo II Interbody Fusion Device System
- K143518 — Valeo Spacer System and Valeo II Interbody Fusion Device System
- K142264 — Valeo C Spacer System, Valeo II C IBF Device
- K142347 — Amedica Valeo II Interbody Fusion Device
- K121892 — PHANTOM PLUS CERAMIC CAGE SYSTEM
- K091278 — VALEO SPACER SYSTEM
- K082037 — SEEPLATE CERVICAL PLATE SYSTEM
- K073430 — VALEO PEDICLE SCREW SPINAL SYSTEM
- K073505 — MODIFICATION TO VALEO VBR
- K073125 — VALEO VBR
- K072022 — VALEO PEDICLE SCREW SPINAL SYSTEM
- K071990 — VALEO CERVICAL PLATE SYSTEM
- K051525 — ARX SPINAL SYSTEM
- K050699 — MODIFICATION TO: VENTED CEMENT RESTRICTOR, MODEL 60102-000-001/004
- K022729 — VENTED CEMENT RESTRICTOR
Data sourced from openFDA. This site is unofficial and independent of the FDA.