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FDA 510(k)

MIS IMPLANT SYSTEM DECIVE

K-Number: K003191 · 2001-09-28

Decision Date2001-09-28
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MIS IMPLANT SYSTEM DECIVE is the device name listed in this FDA 510(k) record. The listed applicant is Mis Implants Technologies , Ltd.. It received FDA 510(k) clearance on 2001-09-28 under 510(k) number K003191. The device is classified under product code DZE. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MIS IMPLANT SYSTEM DECIVE?

MIS IMPLANT SYSTEM DECIVE is a medical device that received FDA 510(k) clearance on 2001-09-28. The listed applicant is Mis Implants Technologies , Ltd.. The 510(k) number is K003191.

When did MIS IMPLANT SYSTEM DECIVE receive FDA 510(k) clearance?

MIS IMPLANT SYSTEM DECIVE received FDA 510(k) clearance on 2001-09-28, under 510(k) number K003191.

Who is the listed applicant for MIS IMPLANT SYSTEM DECIVE?

The FDA 510(k) record lists Mis Implants Technologies , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MIS IMPLANT SYSTEM DECIVE?

The FDA product code for MIS IMPLANT SYSTEM DECIVE is DZE.

Related Clinical Trials

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.

Other records listing Mis Implants Technologies , Ltd. 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.

View all 13 devices →

Related Devices (Code: DZE)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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