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FDA 510(k)

T-PLATE ANTERIOR FIXATION SYSTEM

K-Number: K051764 · 2005-07-13

ApplicantEsm Technologies
Decision Date2005-07-13
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

T-PLATE ANTERIOR FIXATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Esm Technologies. It received FDA 510(k) clearance on 2005-07-13 under 510(k) number K051764. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the T-PLATE ANTERIOR FIXATION SYSTEM?

T-PLATE ANTERIOR FIXATION SYSTEM is a medical device that received FDA 510(k) clearance on 2005-07-13. The listed applicant is Esm Technologies. The 510(k) number is K051764.

When did T-PLATE ANTERIOR FIXATION SYSTEM receive FDA 510(k) clearance?

T-PLATE ANTERIOR FIXATION SYSTEM received FDA 510(k) clearance on 2005-07-13, under 510(k) number K051764.

Who is the listed applicant for T-PLATE ANTERIOR FIXATION SYSTEM?

The FDA 510(k) record lists Esm Technologies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for T-PLATE ANTERIOR FIXATION SYSTEM?

The FDA product code for T-PLATE ANTERIOR FIXATION SYSTEM is KWQ.

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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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