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FDA 510(k)

MINIMATIC VARIOUS IMPLANT SYSTEMS

K-Number: K952905 · 1997-04-16

Decision Date1997-04-16
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MINIMATIC VARIOUS IMPLANT SYSTEMS is the device name listed in this FDA 510(k) record. The listed applicant is Minimatic, Inc.. It received FDA 510(k) clearance on 1997-04-16 under 510(k) number K952905. 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 MINIMATIC VARIOUS IMPLANT SYSTEMS?

MINIMATIC VARIOUS IMPLANT SYSTEMS is a medical device that received FDA 510(k) clearance on 1997-04-16. The listed applicant is Minimatic, Inc.. The 510(k) number is K952905.

When did MINIMATIC VARIOUS IMPLANT SYSTEMS receive FDA 510(k) clearance?

MINIMATIC VARIOUS IMPLANT SYSTEMS received FDA 510(k) clearance on 1997-04-16, under 510(k) number K952905.

Who is the listed applicant for MINIMATIC VARIOUS IMPLANT SYSTEMS?

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

What is the FDA product code for MINIMATIC VARIOUS IMPLANT SYSTEMS?

The FDA product code for MINIMATIC VARIOUS IMPLANT SYSTEMS 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.

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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