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FDA 510(k)

MICROFENESTRATED HIP REPLACEMENT COMPON.

K-Number: K770161 · 1977-01-26

ApplicantMedishield, Inc.
Decision Date1977-01-26
Product CodeJDG
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MICROFENESTRATED HIP REPLACEMENT COMPON. is the device name listed in this FDA 510(k) record. The listed applicant is Medishield, Inc.. It received FDA 510(k) clearance on 1977-01-26 under 510(k) number K770161. The device is classified under product code JDG. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICROFENESTRATED HIP REPLACEMENT COMPON.?

MICROFENESTRATED HIP REPLACEMENT COMPON. is a medical device that received FDA 510(k) clearance on 1977-01-26. The listed applicant is Medishield, Inc.. The 510(k) number is K770161.

When did MICROFENESTRATED HIP REPLACEMENT COMPON. receive FDA 510(k) clearance?

MICROFENESTRATED HIP REPLACEMENT COMPON. received FDA 510(k) clearance on 1977-01-26, under 510(k) number K770161.

Who is the listed applicant for MICROFENESTRATED HIP REPLACEMENT COMPON.?

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

What is the FDA product code for MICROFENESTRATED HIP REPLACEMENT COMPON.?

The FDA product code for MICROFENESTRATED HIP REPLACEMENT COMPON. is JDG.

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Other records listing Medishield, Inc. 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.

K781103SPECTRASCANK780645HMD-2000 BATTERY-POWERED MINI-DRILL, THEK780646AIR-PWOERED COLDRILLK780202MONOMER EVACUATION SYSTEMK761020ANKLE (FREEMAN-SWANSON)K761021ANKLE INSTRUMENTS (FREEMAN-SWANSON)

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Related Devices (Code: JDG)

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.

K212431Biomet Answer/Impact/Integral Distal Centralizer/Centering SleeveBiomet, Inc.K193546Distal CentralizersBiomet, Inc.K173499Exeter V40 Femoral Stem Hip System, Orthinox V40 Femoral HeadsStryker OrthopaedicsK001984PROGENY FORGED COCR CEMENTED FEMORAL COMPONENTStelkast CompanyK992234THE TAPER-FIT TOTAL HIP SYSTEMCorin USAK962002AURA HIP SYSTEM CALCAR REPLACEMENT FEMORAL STEMExactech, 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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