FDA 510(k)

TIGERPAW SYSTEM

K-Number: K101961 · 2010-10-29

Decision Date2010-10-29

Product CodeGDW

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

TIGERPAW SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Laax, Inc.. It received FDA 510(k) clearance on 2010-10-29 under 510(k) number K101961. The device is classified under product code GDW. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIGERPAW SYSTEM?

TIGERPAW SYSTEM is a medical device that received FDA 510(k) clearance on 2010-10-29. The listed applicant is Laax, Inc.. The 510(k) number is K101961.

When did TIGERPAW SYSTEM receive FDA 510(k) clearance?

TIGERPAW SYSTEM received FDA 510(k) clearance on 2010-10-29, under 510(k) number K101961.

Who is the listed applicant for TIGERPAW SYSTEM?

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

What is the FDA product code for TIGERPAW SYSTEM?

The FDA product code for TIGERPAW SYSTEM is GDW.

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Other records listing Laax, Inc. as applicant

K111064TIGERPAW SYSTEM II

Related Devices (Code: GDW)

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.