DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00— 510(k) K062391

Name: FDA 510(k) clearance K062391
Creator: U.S. Food and Drug Administration
Published: 2006-09-14

Substantially Equivalent

Triage Medical, Inc.

FDA 510(k) clearance K062391 for DISPOSABLE POSTERIOR LUMBAR STABILIZATION PROCEDURE KIT, MODELS 9045-01 AND 9045-02; COMPRESSION TOOL, MODEL 6113-00, Substantially Equivalent on 2006-09-14. Applicant: Triage Medical, Inc.. Device class: Unclassified.

Clearance details

Applicant: Triage Medical, Inc.
Product code: Code MRW
Device class: Unclassified
Advisory panel: Unknown
Date received: 2006-08-16
Decision date: 2006-09-14
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Irvine, CA, US

Download summary PDF View on FDA.gov ↗

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