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FDA 510(k)

SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM

K-Number: K031555 · 2003-07-08

ApplicantSynthes (Usa)
Decision Date2003-07-08
Product CodeLXC
DecisionSubstantially Equivalent

Device Summary

SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Synthes (Usa). It received FDA 510(k) clearance on 2003-07-08 under 510(k) number K031555. The device is classified under product code LXC. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM?

SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM is a medical device that received FDA 510(k) clearance on 2003-07-08. The listed applicant is Synthes (Usa). The 510(k) number is K031555.

When did SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM receive FDA 510(k) clearance?

SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM received FDA 510(k) clearance on 2003-07-08, under 510(k) number K031555.

Who is the listed applicant for SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM?

The FDA 510(k) record lists Synthes (Usa) as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM?

The FDA product code for SYNTHES (USA) COMPARTMENTAL PRESSURE MONITORING SYSTEM is LXC.

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Other records listing Synthes (Usa) as applicant

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Related Devices (Code: LXC)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K251900MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K242997MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K223509Compremium Compartment Compressibility Monitoring System (CPM#1)Compremium AGK220952MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K210525MY01 Continuous Compartmental Pressure MonitorMY01, Inc.K202635MY01 Continuous Compartmental Pressure MonitorMY01, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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