FDA 510(k)

SKELETAL FIXATION PIN

K-Number: K895173 · 1989-09-12

Decision Date1989-09-12

Product CodeJDW

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

SKELETAL FIXATION PIN is the device name listed in this FDA 510(k) record. The listed applicant is Kronner Medical. It received FDA 510(k) clearance on 1989-09-12 under 510(k) number K895173. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SKELETAL FIXATION PIN?

SKELETAL FIXATION PIN is a medical device that received FDA 510(k) clearance on 1989-09-12. The listed applicant is Kronner Medical. The 510(k) number is K895173.

When did SKELETAL FIXATION PIN receive FDA 510(k) clearance?

SKELETAL FIXATION PIN received FDA 510(k) clearance on 1989-09-12, under 510(k) number K895173.

Who is the listed applicant for SKELETAL FIXATION PIN?

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

What is the FDA product code for SKELETAL FIXATION PIN?

The FDA product code for SKELETAL FIXATION PIN is JDW.

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_RECRUITING NCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITING NCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDED NCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Kronner Medical as applicant

K894228KRONNER SPHERICAL CUTTERS K895171BLOOD GAS SAFETY SYRINGE K895172KRONNER SACRAL PIN GUIDE K871248KRONNER COLLES-FOREARM EXTERNAL FIXATION K871249KRONNER BI-PLANER TIBIA EXTERNAL FIXATION K871247KRONNER UNIVERSAL FRAME EXTERNAL FIXATION

View all 7 devices →

Related Devices (Code: JDW)

K260073XT3 System; XT3 System, Mini; XT3 System, 40mm; XT3 System, Mini, 40mmBiodynamik, Inc.K250316Meduloc Intramedullary Fracture Fixation (IFF) SystemMeduloc, LLC K241357XT3 SystemBiodynamik, Inc.K223112MAVERICK Mini External Fixation SystemSmith & Nephew, Inc.K213874MAVERICK External Fixation SystemSmith & Nephew, Inc.K211508Steinmann Pins and Kirschner WiresStryker 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.