Simplify Disc— 510(k) K211757

Substantially Equivalent

Nuvasive, Inc.

FDA 510(k) clearance K211757 for Simplify Disc, Substantially Equivalent on 2021-08-20. Applicant: Nuvasive, Inc.. Device class: 2.

Clearance details

Applicant: Nuvasive, Inc.
Product code: Code QLQ
Device class: Class 2
Regulation: 21 CFR 888.4515
Advisory panel: Orthopedic
Date received: 2021-06-07
Decision date: 2021-08-20
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Sunnyvale, CA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QLQ

K262639 — BAGUERA® C Cervical Disc Surgical Instruments2026-08-14
K253392 — Synergy Disc Instruments2026-03-27
K250554 — prodisc® L Instruments2025-04-25
K242869 — prodisc® L Instruments2024-12-17
K241117 — M6-C Single Use, Disposable Instrumentation2024-06-21

More clearances from Nuvasive, Inc.

K240507 — NuVasive AttraX Scaffold2024-03-20
K223731 — NuVasive Modulus-C Interbody System2023-01-12
K173117 — NuVasive® VersaTie System2017-12-07
K141665 — NuVasive CoRoent System2015-03-13
K142205 — NuVasive X-CORE(R) Expandable VBR System2015-02-20

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