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FDA 510(k)

CROSSTREES PVA POD

K-Number: K133372 · 2013-12-06

ApplicantCrosstrees Medical, Inc.
Decision Date2013-12-06
Product CodeNDN
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CROSSTREES PVA POD is the device name listed in this FDA 510(k) record. The listed applicant is Crosstrees Medical, Inc.. It received FDA 510(k) clearance on 2013-12-06 under 510(k) number K133372. The device is classified under product code NDN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CROSSTREES PVA POD?

CROSSTREES PVA POD is a medical device that received FDA 510(k) clearance on 2013-12-06. The listed applicant is Crosstrees Medical, Inc.. The 510(k) number is K133372.

When did CROSSTREES PVA POD receive FDA 510(k) clearance?

CROSSTREES PVA POD received FDA 510(k) clearance on 2013-12-06, under 510(k) number K133372.

Who is the listed applicant for CROSSTREES PVA POD?

The FDA 510(k) record lists Crosstrees Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CROSSTREES PVA POD?

The FDA product code for CROSSTREES PVA POD is NDN.

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.

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Other records listing Crosstrees Medical, Inc. 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.

K130089CROSSTREES PVA POD

Related Devices (Code: NDN)

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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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