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)

AUSTIN MOORE HIP PROSTHESIS

K-Number: K863896 · 1986-11-19

ApplicantKirschner Medical Corp.
Decision Date1986-11-19
Product Code
DecisionSubstantially Equivalent

Device Summary

AUSTIN MOORE HIP PROSTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Kirschner Medical Corp.. It received FDA 510(k) clearance on 1986-11-19 under 510(k) number K863896. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AUSTIN MOORE HIP PROSTHESIS?

AUSTIN MOORE HIP PROSTHESIS is a medical device that received FDA 510(k) clearance on 1986-11-19. The listed applicant is Kirschner Medical Corp.. The 510(k) number is K863896.

When did AUSTIN MOORE HIP PROSTHESIS receive FDA 510(k) clearance?

AUSTIN MOORE HIP PROSTHESIS received FDA 510(k) clearance on 1986-11-19, under 510(k) number K863896.

Who is the listed applicant for AUSTIN MOORE HIP PROSTHESIS?

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

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 Kirschner Medical Corp. 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.

K940537KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEMK936274KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEMK942891SUMMIT TOTAL HIP SYSTEMK941486INTEGRITY TOTAL HIP SYSTEM, NON-POROUSK933843LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATEDK935951KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM

View all 76 devices →

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.

↑