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FDA 510(k)

AAP APS SYSTEM

K-Number: K071852 · 2007-08-29

ApplicantAap Implantate AG
Decision Date2007-08-29
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

AAP APS SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Aap Implantate AG. It received FDA 510(k) clearance on 2007-08-29 under 510(k) number K071852. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AAP APS SYSTEM?

AAP APS SYSTEM is a medical device that received FDA 510(k) clearance on 2007-08-29. The listed applicant is Aap Implantate AG. The 510(k) number is K071852.

When did AAP APS SYSTEM receive FDA 510(k) clearance?

AAP APS SYSTEM received FDA 510(k) clearance on 2007-08-29, under 510(k) number K071852.

Who is the listed applicant for AAP APS SYSTEM?

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 APS SYSTEM?

The FDA product code for AAP APS SYSTEM is KTT.

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.

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Related Devices (Code: KTT)

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.

K254087MAXFRAME AUTOSTRUT™ with Bluetooth Multi-Axial Correction SystemSynthes (USA) Products, LLCK260900DYNEX® External Fixation SystemsVilex, LLCK260112QuikFix External Fixator: Knee-Spanning PackStabiliz Orthopaedics, Inc.K253291Excelsior SystemBlue Ocean GlobalK253613Monkey Rings External Ring Fixation SystemParagon 28, Inc.K253202Hoffmann LRF SystemStryker GmbH

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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