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)

TiLink-P Joint Fusion System

K-Number: K242414 · 2024-11-21

Decision Date2024-11-21
Product CodeOUR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TiLink-P Joint Fusion System is the device name listed in this FDA 510(k) record. The listed applicant is SurGenTec, LLC. It received FDA 510(k) clearance on 2024-11-21 under 510(k) number K242414. The device is classified under product code OUR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TiLink-P Joint Fusion System?

TiLink-P Joint Fusion System is a medical device that received FDA 510(k) clearance on 2024-11-21. The listed applicant is SurGenTec, LLC. The 510(k) number is K242414.

When did TiLink-P Joint Fusion System receive FDA 510(k) clearance?

TiLink-P Joint Fusion System received FDA 510(k) clearance on 2024-11-21, under 510(k) number K242414.

Who is the listed applicant for TiLink-P Joint Fusion System?

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

What is the FDA product code for TiLink-P Joint Fusion System?

The FDA product code for TiLink-P Joint Fusion System is OUR.

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.

Other records listing SurGenTec, LLC 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.

View all 29 devices →

Related Devices (Code: OUR)

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.

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.