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FDA 510(k)

INSERTION TOOLS

K-Number: K891617 · 1989-05-01

Decision Date1989-05-01
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INSERTION TOOLS is the device name listed in this FDA 510(k) record. The listed applicant is Implant Innovations International, Inc.. It received FDA 510(k) clearance on 1989-05-01 under 510(k) number K891617. 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 INSERTION TOOLS?

INSERTION TOOLS is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K891617.

When did INSERTION TOOLS receive FDA 510(k) clearance?

INSERTION TOOLS received FDA 510(k) clearance on 1989-05-01, under 510(k) number K891617.

Who is the listed applicant for INSERTION TOOLS?

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

What is the FDA product code for INSERTION TOOLS?

The FDA product code for INSERTION TOOLS 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 Implant Innovations International, Inc. 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 18 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

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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