Spineology Interbody Fusion System— 510(k) DEN200010

Unknown

Spineology, Inc.

FDA 510(k) clearance DEN200010 for Spineology Interbody Fusion System, Unknown on 2020-09-18. Applicant: Spineology, Inc.. Device class: 2.

Clearance details

Applicant: Spineology, Inc.
Product code: Code OQB
Device class: Class 2
Regulation: 21 CFR 888.3085
Advisory panel: Orthopedic
Date received: 2020-02-19
Decision date: 2020-09-18
Decision: Unknown
Clearance type: Direct
Location: Saint Paul, MN, US

View on FDA.gov ↗

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