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FDA 510(k)

VITALOCK SPIKED ACETABULAR SHELL

K-Number: K953664 · 1995-10-23

ApplicantHowmedica Corp.
Decision Date1995-10-23
Product CodeLPH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VITALOCK SPIKED ACETABULAR SHELL is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-10-23 under 510(k) number K953664. 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 VITALOCK SPIKED ACETABULAR SHELL?

VITALOCK SPIKED ACETABULAR SHELL is a medical device that received FDA 510(k) clearance on 1995-10-23. The listed applicant is Howmedica Corp.. The 510(k) number is K953664.

When did VITALOCK SPIKED ACETABULAR SHELL receive FDA 510(k) clearance?

VITALOCK SPIKED ACETABULAR SHELL received FDA 510(k) clearance on 1995-10-23, under 510(k) number K953664.

Who is the listed applicant for VITALOCK SPIKED ACETABULAR SHELL?

The FDA 510(k) record lists Howmedica Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VITALOCK SPIKED ACETABULAR SHELL?

The FDA product code for VITALOCK SPIKED ACETABULAR SHELL is LPH.

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Other records listing Howmedica Corp. as applicant

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K983528MICRO DYNAMIC MESHK983404TYPE 3 FEMORAL COMPONENTSK980926DURATION II ACETABULAR COMPONENTS-ETHYLENE OXIDE STERILIZATIONK980925DURATION II TIBIAL INSERTS-ETHYLENE OXIDE STERILIZATIONK980626DURATION II ACETABULAR COMPONENTS-GAS PLASMA STERILIZATIONK980632DURATION II TIBIAL INSERTS - GAS PLASMA STERILIZATION

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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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