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FDA 510(k)

OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION)

K-Number: K963959 · 1996-12-19

ApplicantOsteonics Corp.
Decision Date1996-12-19
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION) is the device name listed in this FDA 510(k) record. The listed applicant is Osteonics Corp.. It received FDA 510(k) clearance on 1996-12-19 under 510(k) number K963959. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION)?

OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION) is a medical device that received FDA 510(k) clearance on 1996-12-19. The listed applicant is Osteonics Corp.. The 510(k) number is K963959.

When did OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION) receive FDA 510(k) clearance?

OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION) received FDA 510(k) clearance on 1996-12-19, under 510(k) number K963959.

Who is the listed applicant for OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION)?

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

What is the FDA product code for OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION)?

The FDA product code for OSTEONICS MODULAR ACETABULAR CUP (HA-COATED VERSION) is MEH.

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Other records listing Osteonics Corp. 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.

K983657OSTEONICS SERIES 7000 AD TIBIAL TRAYK980070OSTEONICS HA-COATED DEVICESK984375OSTEONICS SPINAL SYSTEM - SACRAL OFFSET CONNECTOR ASSEMBLYK982798OSTEONICS ANTERIOR CERVICAL COMPRESSION PLATING SYSTEMK984585OSTEONICS +10 UNIPOLAR ADAPTOR SLEEVEK990203OSTEONICS PRIMARY SECUR-FIT PLUS HIP STEMS

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Related Devices (Code: MEH)

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.

K261576Icona Hip StemCorin, Ltd.K250375Allure Hip Stem and Intramedullary PlugsWaldemar Link GmbH & Co. KGK251166Mfinity Femoral SystemMedacta International S.A.K251052Trivicta® Hip StemOrtho Development Corp.K242315Resolve Modular Revision Hip StemUnited Orthopedic CorporationK243839Alteon® HA Femoral StemsExactech, 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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