KOMPREDA— 510(k) K120597

Substantially Equivalent

Custom Spine, Inc.

FDA 510(k) clearance K120597 for KOMPREDA, Substantially Equivalent on 2013-05-03. Applicant: Custom Spine, Inc.. Device class: Unclassified.

Clearance details

Applicant: Custom Spine, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2012-02-28
Decision date: 2013-05-03
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Parsippany, NJ, 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.