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FDA 510(k)

MT-2

K-Number: K961384 · 1996-09-25

ApplicantThe Emerging Technologies Group
Decision Date1996-09-25
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MT-2 is the device name listed in this FDA 510(k) record. The listed applicant is The Emerging Technologies Group. It received FDA 510(k) clearance on 1996-09-25 under 510(k) number K961384. 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 MT-2?

MT-2 is a medical device that received FDA 510(k) clearance on 1996-09-25. The listed applicant is The Emerging Technologies Group. The 510(k) number is K961384.

When did MT-2 receive FDA 510(k) clearance?

MT-2 received FDA 510(k) clearance on 1996-09-25, under 510(k) number K961384.

Who is the listed applicant for MT-2?

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

What is the FDA product code for MT-2?

The FDA product code for MT-2 is DZE.

Other records listing The Emerging Technologies Group 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.

K961381KIS-III NON-SUBMERGED IMPLANT, SCREWS AND CYLINDERSK961382MT1AK961387MT-XK961383MT1K961385MT-3AK961386MT-2A

View all 7 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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, 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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