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FDA 510(k)

TEMPORARY BRIDGE HEAD

K-Number: K871953 · 1987-07-31

ApplicantImplant Innovations International, Inc.
Decision Date1987-07-31
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TEMPORARY BRIDGE HEAD 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 1987-07-31 under 510(k) number K871953. 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 TEMPORARY BRIDGE HEAD?

TEMPORARY BRIDGE HEAD is a medical device that received FDA 510(k) clearance on 1987-07-31. The listed applicant is Implant Innovations International, Inc.. The 510(k) number is K871953.

When did TEMPORARY BRIDGE HEAD receive FDA 510(k) clearance?

TEMPORARY BRIDGE HEAD received FDA 510(k) clearance on 1987-07-31, under 510(k) number K871953.

Who is the listed applicant for TEMPORARY BRIDGE HEAD?

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 TEMPORARY BRIDGE HEAD?

The FDA product code for TEMPORARY BRIDGE HEAD is DZE.

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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.

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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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