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)

Zimmer Segmental System Proximal Femoral Component

K-Number: K183136 · 2019-01-30

ApplicantZimmer, Inc.
Decision Date2019-01-30
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Zimmer Segmental System Proximal Femoral Component is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 2019-01-30 under 510(k) number K183136. 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 Zimmer Segmental System Proximal Femoral Component?

Zimmer Segmental System Proximal Femoral Component is a medical device that received FDA 510(k) clearance on 2019-01-30. The listed applicant is Zimmer, Inc.. The 510(k) number is K183136.

When did Zimmer Segmental System Proximal Femoral Component receive FDA 510(k) clearance?

Zimmer Segmental System Proximal Femoral Component received FDA 510(k) clearance on 2019-01-30, under 510(k) number K183136.

Who is the listed applicant for Zimmer Segmental System Proximal Femoral Component?

The FDA 510(k) record lists Zimmer, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for Zimmer Segmental System Proximal Femoral Component?

The FDA product code for Zimmer Segmental System Proximal Femoral Component is LZO.

Other records listing Zimmer, Inc. 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 80 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.