Z1 Hip System
K-Number: K251906 · 2025-07-18
ApplicantZimmer, Inc.
Decision Date2025-07-18
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Z1 Hip System is a medical device manufactured by Zimmer, Inc.. It received FDA 510(k) clearance on 2025-07-18 under approval number K251906. The device is classified under product code LZO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Z1 Hip System?
Z1 Hip System is a medical device that received FDA 510(k) clearance on 2025-07-18. It is manufactured by Zimmer, Inc.. The 510(k) number is K251906.
When was Z1 Hip System approved by the FDA?
Z1 Hip System received FDA 510(k) clearance on 2025-07-18, under approval number K251906.
What company makes Z1 Hip System?
Z1 Hip System is manufactured by Zimmer, Inc..
What is the FDA product code for Z1 Hip System?
The FDA product code for Z1 Hip System is LZO.
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K172767Zimmer Trabecular Metal Reverse Shoulder System, Mini Glenoid
K172114Zimmer Natural Nail System
K181761Zimmer Biomet Select Ceramic Heads
Related Devices (Code: LZO)
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K160289MasterLoc StemMedacta International
K152903REVIVAL(TM) Modular Revision Hip StemCorin USA
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.