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FDA 510(k)

AESCULAP HYDROLIFT VBR SYSTEM

K-Number: K083186 · 2010-03-04

ApplicantAesculap Implant System, Inc.
Decision Date2010-03-04
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AESCULAP HYDROLIFT VBR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aesculap Implant System, Inc.. It received FDA 510(k) clearance on 2010-03-04 under 510(k) number K083186. 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 AESCULAP HYDROLIFT VBR SYSTEM?

AESCULAP HYDROLIFT VBR SYSTEM is a medical device that received FDA 510(k) clearance on 2010-03-04. The listed applicant is Aesculap Implant System, Inc.. The 510(k) number is K083186.

When did AESCULAP HYDROLIFT VBR SYSTEM receive FDA 510(k) clearance?

AESCULAP HYDROLIFT VBR SYSTEM received FDA 510(k) clearance on 2010-03-04, under 510(k) number K083186.

Who is the listed applicant for AESCULAP HYDROLIFT VBR SYSTEM?

The FDA 510(k) record lists Aesculap Implant System, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AESCULAP HYDROLIFT VBR SYSTEM?

The FDA product code for AESCULAP HYDROLIFT VBR SYSTEM is MQP.

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Other records listing Aesculap Implant System, Inc. 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.

K122783PLASMAFIT ACETABULAR CUP AND VITELENE INSERTK130887S4C NAVIGATION INSTRUMENTSK123909AESCULAP CESPACE XPK130291S4 SPINAL SYSTEMK122985COLUMBUS REVISION KNEE SYSTEMK112551S4 SPINAL SYSTEM

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Related Devices (Code: MQP)

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.

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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