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FDA 510(k)

SOLITAIRE ANTERIOR SPINAL SYSTEM

K-Number: K062810 · 2006-10-17

ApplicantEbi, L.P.
Decision Date2006-10-17
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SOLITAIRE ANTERIOR SPINAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ebi, L.P.. It received FDA 510(k) clearance on 2006-10-17 under 510(k) number K062810. 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 SOLITAIRE ANTERIOR SPINAL SYSTEM?

SOLITAIRE ANTERIOR SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2006-10-17. The listed applicant is Ebi, L.P.. The 510(k) number is K062810.

When did SOLITAIRE ANTERIOR SPINAL SYSTEM receive FDA 510(k) clearance?

SOLITAIRE ANTERIOR SPINAL SYSTEM received FDA 510(k) clearance on 2006-10-17, under 510(k) number K062810.

Who is the listed applicant for SOLITAIRE ANTERIOR SPINAL SYSTEM?

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

What is the FDA product code for SOLITAIRE ANTERIOR SPINAL SYSTEM?

The FDA product code for SOLITAIRE ANTERIOR SPINAL SYSTEM is MQP.

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Other records listing Ebi, L.P. 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.

K100438POLARIS SPINAL SYSTEM, POLARIS/SYNERGY STRUCTURE ANTERIOR FIXATION SYSTEMK100220POLARIS SPINAL SYSTEMK093880PEANUT GROWTH CONTROL PLATING SYSTEMK092574ESL SPINAL SYSTEMK093057BIOMET VISION FOOTRING SYSTEMK092336C-THRU SPINAL SYSTEM

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Related Devices (Code: MQP)

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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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