prodisc® L Instruments— 510(k) K242869

Substantially Equivalent

Centinel Spine, LLC

FDA 510(k) clearance K242869 for prodisc® L Instruments, Substantially Equivalent on 2024-12-17. Applicant: Centinel Spine, LLC. Device class: 2.

Clearance details

Applicant: Centinel Spine, LLC
Product code: Code QLQ
Device class: Class 2
Regulation: 21 CFR 888.4515
Advisory panel: Orthopedic
Date received: 2024-09-20
Decision date: 2024-12-17
Decision: Substantially Equivalent
Clearance type: Traditional
Location: West Chester, PA, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code QLQ

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More clearances from Centinel Spine, LLC

K221848 — prodisc C SK, prodisc C Nova, and prodisc C Vivo Instruments2022-08-19

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