NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM— 510(k) K002677

Name: FDA 510(k) clearance K002677
Creator: U.S. Food and Drug Administration
Published: 2000-11-13

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K002677 for NUVASIVE INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM, Substantially Equivalent on 2000-11-13. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code BXM
Device class: Class 2
Regulation: 21 CFR 868.2775
Advisory panel: Anesthesiology
Date received: 2000-08-28
Decision date: 2000-11-13
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Diego, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code BXM

view all

K013215 — MODIFIED INS-1 INTRAOPERATIVE NERVE SURVEILLANCE SYSTEM2001-10-16
K921498 — VER MED A10011 PNS DUAL ELEMENT ELECTRODE1993-06-09
K870662 — MODEL SKCK STERILE KNOB COVER KIT1987-10-28

More clearances from Nuvasive, Inc.

view all

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.