Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Locking Cage, Full XPE Cup

K-Number: K163441 · 2017-08-25

Decision Date2017-08-25
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Locking Cage, Full XPE Cup is the device name listed in this FDA 510(k) record. The listed applicant is United Orthopedic Corporation. It received FDA 510(k) clearance on 2017-08-25 under 510(k) number K163441. 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 Locking Cage, Full XPE Cup?

Locking Cage, Full XPE Cup is a medical device that received FDA 510(k) clearance on 2017-08-25. The listed applicant is United Orthopedic Corporation. The 510(k) number is K163441.

When did Locking Cage, Full XPE Cup receive FDA 510(k) clearance?

Locking Cage, Full XPE Cup received FDA 510(k) clearance on 2017-08-25, under 510(k) number K163441.

Who is the listed applicant for Locking Cage, Full XPE Cup?

The FDA 510(k) record lists United Orthopedic Corporation as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Locking Cage, Full XPE Cup?

The FDA product code for Locking Cage, Full XPE Cup is LZO.

Other records listing United Orthopedic Corporation as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 26 devices →

Related Devices (Code: LZO)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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.