SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM— 510(k) K031555

Name: FDA 510(k) clearance K031555
Creator: U.S. Food and Drug Administration
Published: 2003-07-08

Substantially Equivalent

Synthes (Usa)

FDA 510(k) clearance K031555 for SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM, Substantially Equivalent on 2003-07-08. Applicant: Synthes (Usa). Device class: Unclassified.

Clearance details

Applicant: Synthes (Usa)
Product code: Code LXC
Device class: Unclassified
Advisory panel: Unknown
Date received: 2003-05-19
Decision date: 2003-07-08
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Paoli, PA, 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.