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FDA 510(k)

C-THRU SPINAL SYSTEM

K-Number: K092336 · 2009-10-15

ApplicantEbi, L.P.
Decision Date2009-10-15
Product CodeMQP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

C-THRU 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 2009-10-15 under 510(k) number K092336. 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 C-THRU SPINAL SYSTEM?

C-THRU SPINAL SYSTEM is a medical device that received FDA 510(k) clearance on 2009-10-15. The listed applicant is Ebi, L.P.. The 510(k) number is K092336.

When did C-THRU SPINAL SYSTEM receive FDA 510(k) clearance?

C-THRU SPINAL SYSTEM received FDA 510(k) clearance on 2009-10-15, under 510(k) number K092336.

Who is the listed applicant for C-THRU 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 C-THRU SPINAL SYSTEM?

The FDA product code for C-THRU 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 SYSTEMK091381IBEX 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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