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)

HORIZON ORTHOPEDIC PIN PROTECTOR

K-Number: K883576 · 1988-09-30

ApplicantHorizon Medical, Inc.
Decision Date1988-09-30
Product CodeLYT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HORIZON ORTHOPEDIC PIN PROTECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Horizon Medical, Inc.. It received FDA 510(k) clearance on 1988-09-30 under 510(k) number K883576. The device is classified under product code LYT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HORIZON ORTHOPEDIC PIN PROTECTOR?

HORIZON ORTHOPEDIC PIN PROTECTOR is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Horizon Medical, Inc.. The 510(k) number is K883576.

When did HORIZON ORTHOPEDIC PIN PROTECTOR receive FDA 510(k) clearance?

HORIZON ORTHOPEDIC PIN PROTECTOR received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883576.

Who is the listed applicant for HORIZON ORTHOPEDIC PIN PROTECTOR?

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

What is the FDA product code for HORIZON ORTHOPEDIC PIN PROTECTOR?

The FDA product code for HORIZON ORTHOPEDIC PIN PROTECTOR is LYT.

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 Horizon Medical, 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.

K980171DERMASENSE PLUS DISPERSIVE ELECTRODEK944969STERI-LUB LUBRICATION GEL

Related Devices (Code: LYT)

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.

K040363CERAMIC TIPPED SKULL PINThe Jerome Group, Inc.K983685BONE BANDChapel and Assoc.K980594OSTEONICS FX-CABLELOK GRIP COMPONENTSOsteonics Corp.K914812K-CAP-E, STERILEWestcon Orthopedics, Inc.K912762K-CAP-I, STERILEWestcon Orthopedics, Inc.K902053K-CAP-I ORTHOPEDIC FIXATION WIRE CAPWestcon Orthopedics, Inc.

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.

↑