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)

CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS

K-Number: K130343 · 2013-05-28

ApplicantCorin USA
Decision Date2013-05-28
Product CodeLZO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS is the device name listed in this FDA 510(k) record. The listed applicant is Corin USA. It received FDA 510(k) clearance on 2013-05-28 under 510(k) number K130343. 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 CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS?

CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS is a medical device that received FDA 510(k) clearance on 2013-05-28. The listed applicant is Corin USA. The 510(k) number is K130343.

When did CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS receive FDA 510(k) clearance?

CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS received FDA 510(k) clearance on 2013-05-28, under 510(k) number K130343.

Who is the listed applicant for CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS?

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

What is the FDA product code for CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS?

The FDA product code for CORIN TRINITY ACETABULAR SYSTEM WITH EXTRA-LONG HEADS is LZO.

Related Clinical Trials

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Corin USA 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.

K203751OMNIVision systemK202805Optimized Positioning System (OPS) InsightK193545Corin Optimized Positioning System (OPS) FemoralK193042Optimized Positioning System (OPS) ReViewK192656Optimized Positioning System (OPS) InsightK190143LARS AC Band Device

View all 56 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.

K260173M-Vizion Femoral Revision System ExtensionMedacta International S.A.K253948Momentum Acetabular Cup SystemUnited Orthopedic CorporationK261009MobileLink Acetabular Cup System – 40mm ID Inserts (various)Waldemar Link GmbH & Co. KGK260831Z1 Hip SystemZimmer, Inc.K260182Avenir® Müller Stem; Avenir Complete™ Hip SystemZimmer, Inc.K260037implantcast Packaging System UpdateImplantcast GmbH

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.

↑