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FDA 510(k)

VENTED CEMENT RESTRICTOR

K-Number: K022729 · 2002-11-14

ApplicantAmedica Corp.
Decision Date2002-11-14
Product CodeJDX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

VENTED CEMENT RESTRICTOR is the device name listed in this FDA 510(k) record. The listed applicant is Amedica Corp.. It received FDA 510(k) clearance on 2002-11-14 under 510(k) number K022729. The device is classified under product code JDX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VENTED CEMENT RESTRICTOR?

VENTED CEMENT RESTRICTOR is a medical device that received FDA 510(k) clearance on 2002-11-14. The listed applicant is Amedica Corp.. The 510(k) number is K022729.

When did VENTED CEMENT RESTRICTOR receive FDA 510(k) clearance?

VENTED CEMENT RESTRICTOR received FDA 510(k) clearance on 2002-11-14, under 510(k) number K022729.

Who is the listed applicant for VENTED CEMENT RESTRICTOR?

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

What is the FDA product code for VENTED CEMENT RESTRICTOR?

The FDA product code for VENTED CEMENT RESTRICTOR is JDX.

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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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