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FDA 510(k)

THP Hip Fracture Plating System

K-Number: K173826 · 2018-02-07

ApplicantBiomet, Inc.
Decision Date2018-02-07
Product CodeJDO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

THP Hip Fracture Plating System is a medical device manufactured by Biomet, Inc.. It received FDA 510(k) clearance on 2018-02-07 under approval number K173826. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THP Hip Fracture Plating System?

THP Hip Fracture Plating System is a medical device that received FDA 510(k) clearance on 2018-02-07. It is manufactured by Biomet, Inc.. The 510(k) number is K173826.

When was THP Hip Fracture Plating System approved by the FDA?

THP Hip Fracture Plating System received FDA 510(k) clearance on 2018-02-07, under approval number K173826.

What company makes THP Hip Fracture Plating System?

THP Hip Fracture Plating System is manufactured by Biomet, Inc..

What is the FDA product code for THP Hip Fracture Plating System?

The FDA product code for THP Hip Fracture Plating System is JDO.

Related Clinical Trials

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Other Devices by Biomet, Inc.

K161592Persona Partial Knee System K162424Ulna Plating System K161166StageOne Select Cement Spacer Molds for Temporary Hip Replacement K160071StageOne Disposable Cement Spacer Molds for Temporary Hemi-Shoulder Prosthesis K161190G7 Dual Mobility System, Active Articulation System K153657Vanguard XP Knee System

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Related Devices (Code: JDO)

K152686CONQUEST FNSmith & Nephew K172785CONQUEST FNSmith & Nephew K193029CONQUEST FNSmith & Nephew, Inc. K210247OsteoCentric Integrated Hip Fastener SystemOsteocentric Technologies D.B.A. Osteocentric Trauma K213126Smith & Nephew, Inc. Plates and Screws Systems: EVOS, Peri-Loc, D-Rad, TC-100, VLP Mini-Mod, Compression Hip Screw (CHS), CONQUEST FN, and cannulated screwsSmith & Nephew, Inc. K230764OsteoCentric Integrated Hip Fastener SystemOsteoCentric Technologies

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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