AR_N Type Implant System
K-Number: K171297 · 2018-01-31
Device Summary
Frequently Asked Questions
What is the AR_N Type Implant System?
AR_N Type Implant System is a medical device that received FDA 510(k) clearance on 2018-01-31. The listed applicant is Biotem Co., Ltd.. The 510(k) number is K171297.
When did AR_N Type Implant System receive FDA 510(k) clearance?
AR_N Type Implant System received FDA 510(k) clearance on 2018-01-31, under 510(k) number K171297.
Who is the listed applicant for AR_N Type Implant System?
The FDA 510(k) record lists Biotem Co., Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AR_N Type Implant System?
The FDA product code for AR_N Type Implant System is DZE.
Other records listing Biotem Co., 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.
Related Devices (Code: DZE)
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.