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)

RABEA DEVICE, MODEL PXXXXXX

K-Number: K990345 · 1999-07-30

ApplicantSignus Medizintechnik GmbH
Decision Date1999-07-30
Product CodeJDK
Advisory CommitteeSU
DecisionUnknown

Device Summary

RABEA DEVICE, MODEL PXXXXXX is the device name listed in this FDA 510(k) record. The listed applicant is Signus Medizintechnik GmbH. It received FDA 510(k) clearance on 1999-07-30 under 510(k) number K990345. The device is classified under product code JDK. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the RABEA DEVICE, MODEL PXXXXXX?

RABEA DEVICE, MODEL PXXXXXX is a medical device that received FDA 510(k) clearance on 1999-07-30. The listed applicant is Signus Medizintechnik GmbH. The 510(k) number is K990345.

When did RABEA DEVICE, MODEL PXXXXXX receive FDA 510(k) clearance?

RABEA DEVICE, MODEL PXXXXXX received FDA 510(k) clearance on 1999-07-30, under 510(k) number K990345.

Who is the listed applicant for RABEA DEVICE, MODEL PXXXXXX?

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

What is the FDA product code for RABEA DEVICE, MODEL PXXXXXX?

The FDA product code for RABEA DEVICE, MODEL PXXXXXX is JDK.

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 Signus Medizintechnik GmbH 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.

K243188CYLOX® STK241438Signus Tetris™ St; Signus Tetris™ R StK220658COSY Cervicothoracic Occipital Rod-Screw SystemK212755SIGNUS SACRONAIL® Transsacral Stabilization SystemK151704Diplomat® Spinal SystemK131372MOBIS II

View all 21 devices →

Related Devices (Code: JDK)

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.

K210062Mectaplug PE IIMedacta International S.A.K061465KMI CEMENT RESTRICTOR IMPLANTKinetikos Medical, Inc.K061698MODIFICATION TO LIFE SPINE CEMENT RESTRICTORLife SpineK060247LIFE SPINE CEMENT RESTRICTORLife SpineK060132SPINAL USA CEMENT RESTRICTOR SYSTEMSpinal USAK051371INTERBODY INNOVATIONS CEMENT RESTRICTORInterbody Innovations, Llp

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.

↑