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)

LINK SADDLE PROTHESIS

K-Number: K943277 · 1995-01-26

ApplicantTurnkey Intergration USA, Inc.
Decision Date1995-01-26
Product Code
DecisionSubstantially Equivalent

Device Summary

LINK SADDLE PROTHESIS is the device name listed in this FDA 510(k) record. The listed applicant is Turnkey Intergration USA, Inc.. It received FDA 510(k) clearance on 1995-01-26 under 510(k) number K943277. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LINK SADDLE PROTHESIS?

LINK SADDLE PROTHESIS is a medical device that received FDA 510(k) clearance on 1995-01-26. The listed applicant is Turnkey Intergration USA, Inc.. The 510(k) number is K943277.

When did LINK SADDLE PROTHESIS receive FDA 510(k) clearance?

LINK SADDLE PROTHESIS received FDA 510(k) clearance on 1995-01-26, under 510(k) number K943277.

Who is the listed applicant for LINK SADDLE PROTHESIS?

The FDA 510(k) record lists Turnkey Intergration USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

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 Turnkey Intergration USA, Inc. 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.

K991405OMNI-FIX, HUMERAL NAILK990523B2C, ESPACE REVISION CUP SYSTEMK990307OMNI-FIX, NAIL SYSTEMK972411LINK CEMENT PLUGK970284ARTOS, DIPLOS SYSTEMK970084LINK CERCLAGE WIRE SYSTEM

View all 26 devices →

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.

↑