TiLink-P Joint Fusion System
K-Number: K242414 · 2024-11-21
Device Summary
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.
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.