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FDA 510(k)

Hoffman LRF System

K-Number: K161753 · 2016-11-15

ApplicantStryker GmbH
Decision Date2016-11-15
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Hoffman LRF System is the device name listed in this FDA 510(k) record. The listed applicant is Stryker GmbH. It received FDA 510(k) clearance on 2016-11-15 under 510(k) number K161753. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Hoffman LRF System?

Hoffman LRF System is a medical device that received FDA 510(k) clearance on 2016-11-15. The listed applicant is Stryker GmbH. The 510(k) number is K161753.

When did Hoffman LRF System receive FDA 510(k) clearance?

Hoffman LRF System received FDA 510(k) clearance on 2016-11-15, under 510(k) number K161753.

Who is the listed applicant for Hoffman LRF System?

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

What is the FDA product code for Hoffman LRF System?

The FDA product code for Hoffman LRF System is KTT.

Other records listing Stryker GmbH as applicant

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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