Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

EBI TOP LOADING MAS SPINAL FIXATION SYSTEM

K-Number: K033312 · 2004-01-13

ApplicantEbi, L.P.
Decision Date2004-01-13
Product CodeNKB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EBI TOP LOADING MAS SPINAL FIXATION 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 2004-01-13 under 510(k) number K033312. The device is classified under product code NKB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBI TOP LOADING MAS SPINAL FIXATION SYSTEM?

EBI TOP LOADING MAS SPINAL FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2004-01-13. The listed applicant is Ebi, L.P.. The 510(k) number is K033312.

When did EBI TOP LOADING MAS SPINAL FIXATION SYSTEM receive FDA 510(k) clearance?

EBI TOP LOADING MAS SPINAL FIXATION SYSTEM received FDA 510(k) clearance on 2004-01-13, under 510(k) number K033312.

Who is the listed applicant for EBI TOP LOADING MAS SPINAL FIXATION 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 EBI TOP LOADING MAS SPINAL FIXATION SYSTEM?

The FDA product code for EBI TOP LOADING MAS SPINAL FIXATION SYSTEM is NKB.

Related Clinical Trials

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.

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.

View all 95 devices →

Related Devices (Code: NKB)

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.

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.

↑