IdentiTi II Cervical Interbody System
K-Number: K251080 · 2025-07-03
Device Summary
Frequently Asked Questions
What is the IdentiTi II Cervical Interbody System?
IdentiTi II Cervical Interbody System is a medical device that received FDA 510(k) clearance on 2025-07-03. The listed applicant is Alphatec Spine, Inc.. The 510(k) number is K251080.
When did IdentiTi II Cervical Interbody System receive FDA 510(k) clearance?
IdentiTi II Cervical Interbody System received FDA 510(k) clearance on 2025-07-03, under 510(k) number K251080.
Who is the listed applicant for IdentiTi II Cervical Interbody System?
The FDA 510(k) record lists Alphatec Spine, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for IdentiTi II Cervical Interbody System?
The FDA product code for IdentiTi II Cervical Interbody System is ODP.
Other records listing Alphatec Spine, 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.
Related Devices (Code: ODP)
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.