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FDA 510(k)

ACETABULAR DOME AND SCREW HOLE PLUGS

K-Number: K920868 · 1992-05-26

ApplicantOsteonics Corp.
Decision Date1992-05-26
Product CodeJDL
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACETABULAR DOME AND SCREW HOLE PLUGS is the device name listed in this FDA 510(k) record. The listed applicant is Osteonics Corp.. It received FDA 510(k) clearance on 1992-05-26 under 510(k) number K920868. The device is classified under product code JDL. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETABULAR DOME AND SCREW HOLE PLUGS?

ACETABULAR DOME AND SCREW HOLE PLUGS is a medical device that received FDA 510(k) clearance on 1992-05-26. The listed applicant is Osteonics Corp.. The 510(k) number is K920868.

When did ACETABULAR DOME AND SCREW HOLE PLUGS receive FDA 510(k) clearance?

ACETABULAR DOME AND SCREW HOLE PLUGS received FDA 510(k) clearance on 1992-05-26, under 510(k) number K920868.

Who is the listed applicant for ACETABULAR DOME AND SCREW HOLE PLUGS?

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 ACETABULAR DOME AND SCREW HOLE PLUGS?

The FDA product code for ACETABULAR DOME AND SCREW HOLE PLUGS is JDL.

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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: JDL)

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.

K073499VERSYS EPOCH FULLCOAT HIP PROSTHESIS, MODEL 4088 SERIESZimmer, Inc.K070785DYNASTY ACETABULAR SYSTEMWrightmedicaltechnologyincK061844DYNASTY ACETABULAR SHELL AND COCR ACETABULAR LINERWrightmedicaltechnologyincK051995PROFEMUR RENAISSANCE HIP STEMWrightmedicaltechnologyincK051348CONSERVE TOTAL FEMORAL HEADWrightmedicaltechnologyincK042841M2A/C2A ACETABULAR SYSTEMBiomet, 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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