NUVASIVE MAXCESS LIGHT GUIDE— 510(k) K042034

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K042034 for NUVASIVE MAXCESS LIGHT GUIDE, Substantially Equivalent on 2004-10-26. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code FST
Device class: Class 2
Regulation: 21 CFR 878.4580
Advisory panel: General, Plastic Surgery
Date received: 2004-07-29
Decision date: 2004-10-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code FST

K200874 — TruView Light Cable, TruView Lateral Retractor Light Cable, Bifurcated Light Cable With Universal End2020-06-30
K141330 — ENDO-CORD2014-12-15
K122637 — LITE DECOMPRESSION SYSTEM- LIGHT CABLE MODEL 480899992012-11-01
K113697 — EIGR SURGICAL ILLUMINATION SYSTEM2012-02-10
K113330 — CABLECAP2012-01-12

More clearances from Nuvasive, Inc.

K240507 — NuVasive AttraX Scaffold2024-03-20
K223731 — NuVasive Modulus-C Interbody System2023-01-12
K211757 — Simplify Disc2021-08-20
K173117 — NuVasive® VersaTie System2017-12-07
K141665 — NuVasive CoRoent System2015-03-13

Data sourced from openFDA. This site is unofficial and independent of the FDA.