Seaspine, Inc.
FDA 510(k) medical device clearances.
Top product codes for Seaspine, Inc.
Recent clearances by Seaspine, Inc.
- K231654 — NorthStar OCT System
- K150469 — Integra Laminoplasty System
- K142488 — SeaSpine Spacer System - (Hollywood, Pacifica, Redondo, Ventura) NanoMetalene, Cambria NanoMetalene , Vu aPOD-L NanoMetalene, Vu ePOD NanoMetalene
- K133418 — INTEGRA EXPANDABLE INTERVEREBRAL BODY FUSION DEVICE (IBD) SYSTEM
- K132859 — INTEGRA FACET FIXATION SYSTEM
- K121924 — INTEGRA INTERSPINOUS PROCESS SYSTEM
- K130830 — INTEGRA LAMINOPLASTY SYSTEM
- K122571 — MALIBU SPINAL SYSTEM WITH THE DAYTONA DEFORMITY SYSTEM
- K112206 — CARDIFF ANTERIOR CERVICAL PLATE SYSTEM
- K111671 — SEASPINE MONOPOLAR PROBE SYSYEM
- K102026 — SEASPINE SPACER SYSTEM
- K103297 — REDONDO-L
- K092521 — ZUMA-C
- K082309 — CAMBRIA
- K083338 — CARDIFF ANTERIOR CERVICAL PLATE SYSTEM
- K083089 — NEWPORT SPINAL SYSTEM
- K082926 — ZUMA, MODEL 55-XXXX/56-XXXX
- K082310 — HOLLYWOOD, PACIFICA, REDONDO, VENTURA
- K072729 — SIERRA
- K080526 — SIERRA SYSTEM
- K072605 — MALIBU SPINAL SYSTEM
- K071726 — ZUMA
- K062934 — SIERRA
- K061342 — MALIBU SPINAL SYSTEM
- K052170 — SEASPINE VBR SYSTEM
- K051942 — MALIBU SPINAL SYSTEM
- K051663 — MALIBU SPINAL SYSTEM
Data sourced from openFDA. This site is unofficial and independent of the FDA.