APTUS 2.0/2.3 FOUR CORNER FUSION PLATE
K-Number: K090983 · 2009-07-01
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Device Summary
Frequently Asked Questions
What is the APTUS 2.0/2.3 FOUR CORNER FUSION PLATE?
APTUS 2.0/2.3 FOUR CORNER FUSION PLATE is a medical device that received FDA 510(k) clearance on 2009-07-01. The listed applicant is Medartis AG. The 510(k) number is K090983.
When did APTUS 2.0/2.3 FOUR CORNER FUSION PLATE receive FDA 510(k) clearance?
APTUS 2.0/2.3 FOUR CORNER FUSION PLATE received FDA 510(k) clearance on 2009-07-01, under 510(k) number K090983.
Who is the listed applicant for APTUS 2.0/2.3 FOUR CORNER FUSION PLATE?
The FDA 510(k) record lists Medartis AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for APTUS 2.0/2.3 FOUR CORNER FUSION PLATE?
The FDA product code for APTUS 2.0/2.3 FOUR CORNER FUSION PLATE is HRS.
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 Medartis AG 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: HRS)
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.
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