ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP
K-Number: K213781 · 2022-01-18
Device Summary
Frequently Asked Questions
What is the ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP?
ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP is a medical device that received FDA 510(k) clearance on 2022-01-18. The listed applicant is Depuy Ireland UC. The 510(k) number is K213781.
When did ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP receive FDA 510(k) clearance?
ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP received FDA 510(k) clearance on 2022-01-18, under 510(k) number K213781.
Who is the listed applicant for ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP?
The FDA 510(k) record lists Depuy Ireland UC as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP?
The FDA product code for ATTUNE® Porous Fixed Bearing Tibial Base with AFFIXIUM™ 3DP is MBH.
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 Depuy Ireland UC 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: MBH)
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.