CPT Hip System
K-Number: K191735 · 2020-03-20
ApplicantZimmer, Inc.
Decision Date2020-03-20
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
CPT Hip System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2020-03-20 under approval number K191735. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the CPT Hip System?
CPT Hip System is a medical device that received FDA 510(k) clearance on 2020-03-20. It is manufactured by Zimmer, Inc.. The 510(k) number is K191735.
When was CPT Hip System approved by the FDA?
CPT Hip System received FDA 510(k) clearance on 2020-03-20, under approval number K191735.
What company makes CPT Hip System?
CPT Hip System is manufactured by Zimmer, Inc..
What is the FDA product code for CPT Hip System?
The FDA product code for CPT Hip System is JDI.
Other Devices by Zimmer, Inc.
K161830Zimmer M/L Taper Hip Prosthesis
K151716Cable-Ready Cable Grip System: Cable-Ready Bone Plate System
K151848Cable-Ready® Cable Grip System: Cable-Ready Pin System, Cable-Ready Needle System
K172767Zimmer Trabecular Metal Reverse Shoulder System, Mini Glenoid
K172114Zimmer Natural Nail System
K181761Zimmer Biomet Select Ceramic Heads
Related Devices (Code: JDI)
K160923REDAPT Anteverted Cemented LinerSmith & Nephew, Inc.
K153057FitRite Total Hip Arthroplasty SystemExcera Orthopedics, Inc.
K153725Corin TaperFit Hip StemCorin U.S.A. Limited
K153216Alpine Cemented Hip SystemOrtho Development Corporation
K162125MALUC Total Hip Arthroplasty SystemSurgtech, Inc.
K180973Libertas Hip Replacement SystemMaxx Orthopedics, Inc.
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.