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FDA 510(k)

ACCIN PATELLOFEMORAL SYSTEM

K-Number: K073120 · 2008-02-29

ApplicantAccelerated Innovation, LLC
Decision Date2008-02-29
Product CodeKRR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACCIN PATELLOFEMORAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Accelerated Innovation, LLC. It received FDA 510(k) clearance on 2008-02-29 under 510(k) number K073120. The device is classified under product code KRR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCIN PATELLOFEMORAL SYSTEM?

ACCIN PATELLOFEMORAL SYSTEM is a medical device that received FDA 510(k) clearance on 2008-02-29. The listed applicant is Accelerated Innovation, LLC. The 510(k) number is K073120.

When did ACCIN PATELLOFEMORAL SYSTEM receive FDA 510(k) clearance?

ACCIN PATELLOFEMORAL SYSTEM received FDA 510(k) clearance on 2008-02-29, under 510(k) number K073120.

Who is the listed applicant for ACCIN PATELLOFEMORAL SYSTEM?

The FDA 510(k) record lists Accelerated Innovation, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACCIN PATELLOFEMORAL SYSTEM?

The FDA product code for ACCIN PATELLOFEMORAL SYSTEM is KRR.

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Other records listing Accelerated Innovation, LLC 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.

K081127ACCIN TOTAL KNEE SYSTEMK080647ACCIN BIPOLAR HEAD SYSTEMK080539ACCIN UNIPOLAR HEAD SYSTEMK073531ACCIN PEDICLE SCREW SYSTEMK073530ACCIN ANTERIOR CERVICAL PLATE SYSTEMK073068ACCIN HIP SYSTEM

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Related Devices (Code: KRR)

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.

K231253Overture Orthopaedics Patellofemoral SystemOverture Resurfacing, Inc.K221048Episealer Patellofemoral SystemEpisurf Medical, Inc.K211303Avon Patello-femoral Joint ProsthesisHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK200122MOTO PFJ SystemMedacta International S.A.K181280Patello-Femoral Wave (Kahuna) Arthroplasty SystemArthrosurface, Inc.K160461Arthrex iBalance BiCompartmental Arthroplasty SystemArthrex, Inc.

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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