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FDA 510(k)

EBI TROCHANTERIC NAIL SYSTEM

K-Number: K050118 · 2005-02-16

ApplicantEbi, L.P.
Decision Date2005-02-16
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EBI TROCHANTERIC NAIL 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 2005-02-16 under 510(k) number K050118. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the EBI TROCHANTERIC NAIL SYSTEM?

EBI TROCHANTERIC NAIL SYSTEM is a medical device that received FDA 510(k) clearance on 2005-02-16. The listed applicant is Ebi, L.P.. The 510(k) number is K050118.

When did EBI TROCHANTERIC NAIL SYSTEM receive FDA 510(k) clearance?

EBI TROCHANTERIC NAIL SYSTEM received FDA 510(k) clearance on 2005-02-16, under 510(k) number K050118.

Who is the listed applicant for EBI TROCHANTERIC NAIL 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 TROCHANTERIC NAIL SYSTEM?

The FDA product code for EBI TROCHANTERIC NAIL SYSTEM is HSB.

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Other records listing Ebi, L.P. as applicant

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Related Devices (Code: HSB)

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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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