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 a medical device manufactured by Stryker GmbH. It received FDA 510(k) clearance on 2016-11-15 under approval 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. It is manufactured by Stryker GmbH. The 510(k) number is K161753.
When was Hoffman LRF System approved by the FDA?
Hoffman LRF System received FDA 510(k) clearance on 2016-11-15, under approval number K161753.
What company makes Hoffman LRF System?
Hoffman LRF System is manufactured by Stryker GmbH.
What is the FDA product code for Hoffman LRF System?
The FDA product code for Hoffman LRF System is KTT.
Related Clinical Trials
Other Devices by Stryker GmbH
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K151881X-Fix Line AdditionsVilex IN Tennessee, Inc.
K151580D.N.E. External Fixation SystemDne, LLC
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.