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FDA 510(k)

Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray

K-Number: K172849 · 2017-11-16

ApplicantIntellijoint Surgical, Inc.
Decision Date2017-11-16
Product CodeOLO
Advisory CommitteeNE
DecisionSubstantially Equivalent

Device Summary

Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray is a medical device manufactured by Intellijoint Surgical, Inc.. It received FDA 510(k) clearance on 2017-11-16 under approval number K172849. The device is classified under product code OLO. It was reviewed by the NE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray?

Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray is a medical device that received FDA 510(k) clearance on 2017-11-16. It is manufactured by Intellijoint Surgical, Inc.. The 510(k) number is K172849.

When was Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray approved by the FDA?

Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray received FDA 510(k) clearance on 2017-11-16, under approval number K172849.

What company makes Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray?

Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray is manufactured by Intellijoint Surgical, Inc..

What is the FDA product code for Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray?

The FDA product code for Intellijoint HIP System (Cart), Intellijoint HIP System (Portable), Intellijoint HIP Instrument Tray is OLO.

Related Clinical Trials

NCT07399574 Diagnostic Accuracy of A Diquat Quantitative Detection Kit and A Portable Mass Spectrometry System for Quantifying Diquat Concentrations in Human Blood Samples NOT_YET_RECRUITING NCT05673408 NIBP Validation Study RECRUITING NCT05150197 Virtual Reality Visual Field Testing as an Alternative in Childhood Eye Disease RECRUITING NCT06868979 Optical Imaging in X-linked Disorders. RECRUITING NCT07231653 Home Monitoring Study for Surgical Patients NOT_YET_RECRUITING NCT04436068 Hyperfine Portable MRI in Hydrocephalus and Other Conditions Prompting Outpatient Brain Imaging ACTIVE_NOT_RECRUITING

Other Devices by Intellijoint Surgical, Inc.

K171525Intellijoint HIP Generation 2B System K162364Intellijoint HIP Generation 2A System K191507Intellijoint® Navigation System K211876Intellijoint VIEW

Related Devices (Code: OLO)

K162375Envision 3D: Image Guidance System7D Surgical, Inc. K162341Stryker OrthoMap Precision Knee systemStryker Leibinger GmbH & Co KG K162195TSolution One Cup1 Surgical SystemTHINK Surgical, Inc. K160385Precision ScrewCryptych Pty, Ltd. K153700Aesculap(R) Implant Systems (AIS) S4 Navigation InstrumentsAesculap Implant Systems, LLC K153240Styrker OrthoMap Express Knee SystemStryker Corporate

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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