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FDA 510(k)

SUMMIT ACETABULAR SYSTEM

K-Number: K983014 · 1998-10-27

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1998-10-27
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SUMMIT ACETABULAR SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1998-10-27 under 510(k) number K983014. 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 SUMMIT ACETABULAR SYSTEM?

SUMMIT ACETABULAR SYSTEM is a medical device that received FDA 510(k) clearance on 1998-10-27. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K983014.

When did SUMMIT ACETABULAR SYSTEM receive FDA 510(k) clearance?

SUMMIT ACETABULAR SYSTEM received FDA 510(k) clearance on 1998-10-27, under 510(k) number K983014.

Who is the listed applicant for SUMMIT ACETABULAR SYSTEM?

The FDA 510(k) record lists Johnson & Johnson Professionals, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SUMMIT ACETABULAR SYSTEM?

The FDA product code for SUMMIT ACETABULAR SYSTEM is LPH.

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Other records listing Johnson & Johnson Professionals, Inc. as applicant

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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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