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FDA 510(k)

MODIFICATION TO: INTERPLATE VBR SYSTEM

K-Number: K071372 · 2007-06-11

ApplicantRsb Spine, LLC
Decision Date2007-06-11
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFICATION TO: INTERPLATE VBR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Rsb Spine, LLC. It received FDA 510(k) clearance on 2007-06-11 under 510(k) number K071372. 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: INTERPLATE VBR SYSTEM?

MODIFICATION TO: INTERPLATE VBR SYSTEM is a medical device that received FDA 510(k) clearance on 2007-06-11. The listed applicant is Rsb Spine, LLC. The 510(k) number is K071372.

When did MODIFICATION TO: INTERPLATE VBR SYSTEM receive FDA 510(k) clearance?

MODIFICATION TO: INTERPLATE VBR SYSTEM received FDA 510(k) clearance on 2007-06-11, under 510(k) number K071372.

Who is the listed applicant for MODIFICATION TO: INTERPLATE VBR SYSTEM?

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

What is the FDA product code for MODIFICATION TO: INTERPLATE VBR SYSTEM?

The FDA product code for MODIFICATION TO: INTERPLATE VBR SYSTEM is MQP.

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Other records listing Rsb Spine, LLC 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.

K092540C-PS PEEK OPTIMA CERVICAL INTERBODY SPACER, L-PS PEEK OPTIMA LUMBAR INTERBODY SPACERK092070INTERPLATE CK081194INTERPLATE PEEK CERVICAL INTERBODY FUSION DEVICE (IFD)K071922INTERPLATE INTERBODY FUSION DEVICE, MODELS C, CGC, L AND LGCK070316INTERPLATE VBR SYSTEMK061401INTERPLATE VBR 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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