AAP ACROPLATE
K-Number: K030909 · 2003-04-10
Advertisement
Device Summary
Frequently Asked Questions
What is the AAP ACROPLATE?
AAP ACROPLATE is a medical device that received FDA 510(k) clearance on 2003-04-10. The listed applicant is Aap Implantate AG. The 510(k) number is K030909.
When did AAP ACROPLATE receive FDA 510(k) clearance?
AAP ACROPLATE received FDA 510(k) clearance on 2003-04-10, under 510(k) number K030909.
Who is the listed applicant for AAP ACROPLATE?
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 ACROPLATE?
The FDA product code for AAP ACROPLATE 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.
Advertisement