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FDA 510(k)

I.T.S. EXTREMITY FIXATION SYSTEMS

K-Number: K131722 · 2013-08-07

ApplicantI.T.S. GmbH
Decision Date2013-08-07
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

I.T.S. EXTREMITY FIXATION SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is I.T.S. GmbH. It received FDA 510(k) clearance on 2013-08-07 under 510(k) number K131722. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the I.T.S. EXTREMITY FIXATION SYSTEMS?

I.T.S. EXTREMITY FIXATION SYSTEMS is a medical device that received FDA 510(k) clearance on 2013-08-07. The listed applicant is I.T.S. GmbH. The 510(k) number is K131722.

When did I.T.S. EXTREMITY FIXATION SYSTEMS receive FDA 510(k) clearance?

I.T.S. EXTREMITY FIXATION SYSTEMS received FDA 510(k) clearance on 2013-08-07, under 510(k) number K131722.

Who is the listed applicant for I.T.S. EXTREMITY FIXATION SYSTEMS?

The FDA 510(k) record lists I.T.S. GmbH as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for I.T.S. EXTREMITY FIXATION SYSTEMS?

The FDA product code for I.T.S. EXTREMITY FIXATION SYSTEMS is HRS.

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.

Other records listing I.T.S. GmbH 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.

Related Devices (Code: HRS)

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.

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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