MIS IMPLANT SYSTEM DECIVE
K-Number: K003191 · 2001-09-28
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Device Summary
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.
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
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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