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)

A.L.P.S. CALCANEAL PLATING SYSTEM

K-Number: K132898 · 2013-11-19

ApplicantBiomet Manufacturing Corp
Decision Date2013-11-19
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

A.L.P.S. CALCANEAL PLATING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing Corp. It received FDA 510(k) clearance on 2013-11-19 under 510(k) number K132898. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the A.L.P.S. CALCANEAL PLATING SYSTEM?

A.L.P.S. CALCANEAL PLATING SYSTEM is a medical device that received FDA 510(k) clearance on 2013-11-19. The listed applicant is Biomet Manufacturing Corp. The 510(k) number is K132898.

When did A.L.P.S. CALCANEAL PLATING SYSTEM receive FDA 510(k) clearance?

A.L.P.S. CALCANEAL PLATING SYSTEM received FDA 510(k) clearance on 2013-11-19, under 510(k) number K132898.

Who is the listed applicant for A.L.P.S. CALCANEAL PLATING SYSTEM?

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

What is the FDA product code for A.L.P.S. CALCANEAL PLATING SYSTEM?

The FDA product code for A.L.P.S. CALCANEAL PLATING SYSTEM is HRS.

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 Biomet Manufacturing 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.

K230540Patient Specific Planning Solution™ 3D Bone ModelsK214001Comprehensive® Shoulder System, Comprehensive® Reverse Shoulder SystemK211729Comprehensive® Convertible Glenoid - Vivacit-E LinerK202232Comprehensive Vault Reconstruction SystemK193038Comprehensive Shoulder SystemK182516Comprehensive Nano Stemless Shoulder

View all 82 devices →

Related Devices (Code: HRS)

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.

K261892ProRib Fixation SystemCosta Surgical, Inc.K262098EnHAnce PEEK Bunion SystemNvision Biomedical TechnologiesK262963TMC Implant Fixation SystemTreace Medical Concepts, Inc.K261647Tempo Plating System; Ultra Compression Screw SystemPace SurgicalK261830FRAXION 3.5 Plate System (Various - See Catalog);FRAXION 4.5 Plate System (Various - See Catalog);FRAXION Mini Plate System (Various - See Catalog);FRAXION Bone Screw System (Various - See Catalog)Ortler Global Tibbi Gerecler Anonim SirketiK262537Versalock Sterile Plating SystemGM Dos Reis Industria e Comercio Ltda.

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.

↑