PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER— 510(k) K090767

Name: FDA 510(k) clearance K090767
Creator: U.S. Food and Drug Administration
Published: 2009-06-11

Unknown

Interventional Spine, Inc.

FDA 510(k) clearance K090767 for PERPOS FCD-2 SYSTEM (SINGLE PATIENT USE), ANCHOR, STABILIZER, Unknown on 2009-06-11. Applicant: Interventional Spine, Inc.. Device class: Unclassified.

Clearance details

Applicant: Interventional Spine, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2009-03-23
Decision date: 2009-06-11
Decision: Unknown
Clearance type: Special
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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