OPTIMESH— 510(k) K014200

Unknown

Spineology, Inc.

FDA 510(k) clearance K014200 for OPTIMESH, Unknown on 2003-11-26. Applicant: Spineology, Inc.. Device class: 2.

Clearance details

Applicant: Spineology, Inc.
Product code: Code EZX
Device class: Class 2
Regulation: 21 CFR 878.3300
Advisory panel: General, Plastic Surgery
Date received: 2001-12-21
Decision date: 2003-11-26
Decision: Unknown
Clearance type: Traditional
Location: Stillwater, MN, US

Download summary PDF View on FDA.gov ↗

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