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FDA 510(k)

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM

K-Number: K020522 · 2002-03-21

ApplicantDepuyacromed
Decision Date2002-03-21
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Depuyacromed. It received FDA 510(k) clearance on 2002-03-21 under 510(k) number K020522. The device is classified under product code MQP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM?

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM is a medical device that received FDA 510(k) clearance on 2002-03-21. The listed applicant is Depuyacromed. The 510(k) number is K020522.

When did MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM received FDA 510(k) clearance on 2002-03-21, under 510(k) number K020522.

Who is the listed applicant for MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM?

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

What is the FDA product code for MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM?

The FDA product code for MODIFICATION TO SURGICAL TITANIUM MESH SYSTEM is MQP.

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Other records listing Depuyacromed as applicant

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.

K040197EAGLE ANTERIOR CERVIAL PLATE SYSTEMK031635DEPUY ACROMED VBR SYSTEMK030833DEPUY ACROMED VBR SYSTEMK030383MODIFICATION TO MOSS MIAMI SPINAL SYSTEM POLYAXIAL SCREWSK030249SURGICAL TITANIUM MESH SYSTEMK030103SUMMIT OCT SPINAL SYSTEM MINIPOLYAXIAL SCREWS

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Related Devices (Code: MQP)

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K261810Vertiwedge® Intraosseous SystemFoundation Surgical GroupK261031POSEIDON STSignus Medinzintechnik GmbHK253158VyBrate™ VBR SystemVy Spine, LLCK241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc.K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AGK233359DOMINION Expandable Corpectomy SystemAstura Medical

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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