ANADIAS ZARA SYSTEM MALAR IMPLANTS
K-Number: K871190 · 1987-04-10
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Device Summary
Frequently Asked Questions
What is the ANADIAS ZARA SYSTEM MALAR IMPLANTS?
ANADIAS ZARA SYSTEM MALAR IMPLANTS is a medical device that received FDA 510(k) clearance on 1987-04-10. The listed applicant is Anadias, Inc.. The 510(k) number is K871190.
When did ANADIAS ZARA SYSTEM MALAR IMPLANTS receive FDA 510(k) clearance?
ANADIAS ZARA SYSTEM MALAR IMPLANTS received FDA 510(k) clearance on 1987-04-10, under 510(k) number K871190.
Who is the listed applicant for ANADIAS ZARA SYSTEM MALAR IMPLANTS?
The FDA 510(k) record lists Anadias, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ANADIAS ZARA SYSTEM MALAR IMPLANTS?
The FDA product code for ANADIAS ZARA SYSTEM MALAR IMPLANTS is FWP.
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 Anadias, 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: FWP)
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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