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FDA 510(k)

TAMARACK ANTERIOR THORACOLUNBAR

K-Number: K050390 · 2005-03-14

ApplicantAlphatec/Nexmed
Decision Date2005-03-14
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TAMARACK ANTERIOR THORACOLUNBAR is the device name listed in this FDA 510(k) record. The listed applicant is Alphatec/Nexmed. It received FDA 510(k) clearance on 2005-03-14 under 510(k) number K050390. 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 TAMARACK ANTERIOR THORACOLUNBAR?

TAMARACK ANTERIOR THORACOLUNBAR is a medical device that received FDA 510(k) clearance on 2005-03-14. The listed applicant is Alphatec/Nexmed. The 510(k) number is K050390.

When did TAMARACK ANTERIOR THORACOLUNBAR receive FDA 510(k) clearance?

TAMARACK ANTERIOR THORACOLUNBAR received FDA 510(k) clearance on 2005-03-14, under 510(k) number K050390.

Who is the listed applicant for TAMARACK ANTERIOR THORACOLUNBAR?

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

What is the FDA product code for TAMARACK ANTERIOR THORACOLUNBAR?

The FDA product code for TAMARACK ANTERIOR THORACOLUNBAR is KWQ.

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Other records listing Alphatec/Nexmed as applicant

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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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