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)

CRADLE FIXATION DEVICE

K-Number: K941772 · 1995-08-07

ApplicantNeoligaments, Ltd.
Decision Date1995-08-07
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CRADLE FIXATION DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Neoligaments, Ltd.. It received FDA 510(k) clearance on 1995-08-07 under 510(k) number K941772. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CRADLE FIXATION DEVICE?

CRADLE FIXATION DEVICE is a medical device that received FDA 510(k) clearance on 1995-08-07. The listed applicant is Neoligaments, Ltd.. The 510(k) number is K941772.

When did CRADLE FIXATION DEVICE receive FDA 510(k) clearance?

CRADLE FIXATION DEVICE received FDA 510(k) clearance on 1995-08-07, under 510(k) number K941772.

Who is the listed applicant for CRADLE FIXATION DEVICE?

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

What is the FDA product code for CRADLE FIXATION DEVICE?

The FDA product code for CRADLE FIXATION DEVICE is JDR.

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 Neoligaments, Ltd. 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.

K952543GRAFTOLOGER PGH & ACL RECONSTRUCTION INSTRUMENT SETK935753THE GRAFTOLOGERK930339REAMER BITK913461FASTLOK (STAPLE & BUCKLE) FIXATION SYSTEMK911445FASTLOK (STAPLE AND BUCKLE) FIXATION SYSTEMK904340FASTLOK (STAPLE AND BUCKLE) FIXATION SYSTEM

View all 7 devices →

Related Devices (Code: JDR)

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.

K262451Arthrex DynaNite StaplesArthrex, Inc.K261121Megalodon Dynamic Compression SystemParagon 28, Inc.K250712Linkt Compression Staple SystemTrax SurgicalK243888Medline UNITE® REFLEX® Hybrid Nitinol Implant SystemMedline Industries, LPK243742Arthrex DynaNite Nitinol StaplesArthrex, Inc.K243658TMC Compression Implant SystemTreace Medical Concepts

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.

↑