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FDA 510(k)

IMPLANT LOCATION SOFTWARE-T

K-Number: K070713 · 2007-05-02

ApplicantTactile Technologies, Ltd.
Decision Date2007-05-02
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

IMPLANT LOCATION SOFTWARE-T is the device name listed in this FDA 510(k) record. The listed applicant is Tactile Technologies, Ltd.. It received FDA 510(k) clearance on 2007-05-02 under 510(k) number K070713. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANT LOCATION SOFTWARE-T?

IMPLANT LOCATION SOFTWARE-T is a medical device that received FDA 510(k) clearance on 2007-05-02. The listed applicant is Tactile Technologies, Ltd.. The 510(k) number is K070713.

When did IMPLANT LOCATION SOFTWARE-T receive FDA 510(k) clearance?

IMPLANT LOCATION SOFTWARE-T received FDA 510(k) clearance on 2007-05-02, under 510(k) number K070713.

Who is the listed applicant for IMPLANT LOCATION SOFTWARE-T?

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

What is the FDA product code for IMPLANT LOCATION SOFTWARE-T?

The FDA product code for IMPLANT LOCATION SOFTWARE-T is LLZ.

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Other records listing Tactile Technologies, Ltd. 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.

K050341IMPLANT LOCATION SOFTWARE, MODEL 0.1.0

Related Devices (Code: LLZ)

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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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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