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FDA 510(k)

ACCIN HIP SYSTEM

K-Number: K073068 · 2008-01-10

ApplicantAccelerated Innovation, LLC
Decision Date2008-01-10
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACCIN HIP 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 2008-01-10 under 510(k) number K073068. The device is classified under product code LPH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACCIN HIP SYSTEM?

ACCIN HIP SYSTEM is a medical device that received FDA 510(k) clearance on 2008-01-10. The listed applicant is Accelerated Innovation, LLC. The 510(k) number is K073068.

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

ACCIN HIP SYSTEM received FDA 510(k) clearance on 2008-01-10, under 510(k) number K073068.

Who is the listed applicant for ACCIN HIP 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 HIP SYSTEM?

The FDA product code for ACCIN HIP SYSTEM is LPH.

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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 SYSTEMK073120ACCIN PATELLOFEMORAL SYSTEMK073531ACCIN PEDICLE SCREW SYSTEMK073530ACCIN ANTERIOR CERVICAL PLATE SYSTEM

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Related Devices (Code: LPH)

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.

K261453G7® Acetabular SystemZimmer BiometK253630Mpact 3D Metal FoamMedacta International S.A.K254043TRIVANCE™ Hip StemGlobus Medical, Inc.K261624Omnifit® 20° Series I Insert;Omnifit® Crossfire® 10° Series II Insert; Constrained Acetabular Insert; Trident® Crossfire® 0° Polyethylene Insert; Trident ® Crossfire ® 10° Polyethylene Insert;System 12 Crossfire® 10° Insert; Trident® 0° Constrained Acetabular Insert; Trident® Constrained Acetabular Liner;Trident® All Poly Constrained Acetabular Insert; Crossfire® Eccentric Insert 10°; Artisan® Bone Plug;UHR® Universal Head Bipolar ComponentHowmedica Osteonics Corp., Dba Stryker OrthopaedicsK243192iNSitu Lateralized Acetabular Liners, iNSitu Femoral Stems with Plasma Sprayed CPTi CoatingNextstep Arthopedix, LLCK251270Taperloc® Complete Hip StemBiomet, 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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