AAP BONE PLATES AND SCREW IMPLANTS
K-Number: K072411 · 2008-03-20
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Device Summary
Frequently Asked Questions
What is the AAP BONE PLATES AND SCREW IMPLANTS?
AAP BONE PLATES AND SCREW IMPLANTS is a medical device that received FDA 510(k) clearance on 2008-03-20. The listed applicant is Aap Implantate AG. The 510(k) number is K072411.
When did AAP BONE PLATES AND SCREW IMPLANTS receive FDA 510(k) clearance?
AAP BONE PLATES AND SCREW IMPLANTS received FDA 510(k) clearance on 2008-03-20, under 510(k) number K072411.
Who is the listed applicant for AAP BONE PLATES AND SCREW IMPLANTS?
The FDA 510(k) record lists Aap Implantate AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AAP BONE PLATES AND SCREW IMPLANTS?
The FDA product code for AAP BONE PLATES AND SCREW IMPLANTS 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 Aap Implantate 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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