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)

REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS

K-Number: K012694 · 2002-02-04

ApplicantAdven Medical
Decision Date2002-02-04
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS is the device name listed in this FDA 510(k) record. The listed applicant is Adven Medical. It received FDA 510(k) clearance on 2002-02-04 under 510(k) number K012694. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS?

REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS is a medical device that received FDA 510(k) clearance on 2002-02-04. The listed applicant is Adven Medical. The 510(k) number is K012694.

When did REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS receive FDA 510(k) clearance?

REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS received FDA 510(k) clearance on 2002-02-04, under 510(k) number K012694.

Who is the listed applicant for REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS?

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

What is the FDA product code for REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS?

The FDA product code for REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURS is HWE.

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 Adven Medical 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.

K021528REPROCESSED VENODYNE SEQUENTIAL COMPRESSION SLEEVES / WRAPK013987REPROCESSED DISPOSABLE TROCARSK012675REPROCESSED USED DISPOSABLE SEQUENTIAL COMPRESSION SLEEVES/WRAPSK012676REPROCESSED USED, DISPOSABLE BLADES, BURS, BITS AND TAPSK940501RE-SHARPENABLE SAW BLADES

Related Devices (Code: HWE)

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.

K102743ORTHO SOLUTIONS - STERILE, DRILLS, TAPS, GUIDE PINS & WIRESOrtho Solutions LimitedK063688SURGICAL IRRIGATION SYSTEM, IRRIGATION TUBEThe Anspach Effort, Inc.K050766EXPLANT OSTEONECROSIS INTERVENTION IMPLANT REMOVAL SYSTEMZimmer TrabecularK043310SYNTHES (USA) ELECTRIC PEN DRIVE SYSTEMSynthes (Usa)K022744REPROCESSED USED DISPOSABLE ARTHROSCOPIC BLADES AND BURSMedical Device ServicesK012676REPROCESSED USED, DISPOSABLE BLADES, BURS, BITS AND TAPSAdven Medical

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.

↑