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FDA 510(k)

TC-1111 TRANSFER PIN

K-Number: K903044 · 1990-11-20

Decision Date1990-11-20
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TC-1111 TRANSFER PIN is the device name listed in this FDA 510(k) record. The listed applicant is Minimatic Implant Technology. It received FDA 510(k) clearance on 1990-11-20 under 510(k) number K903044. 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 TC-1111 TRANSFER PIN?

TC-1111 TRANSFER PIN is a medical device that received FDA 510(k) clearance on 1990-11-20. The listed applicant is Minimatic Implant Technology. The 510(k) number is K903044.

When did TC-1111 TRANSFER PIN receive FDA 510(k) clearance?

TC-1111 TRANSFER PIN received FDA 510(k) clearance on 1990-11-20, under 510(k) number K903044.

Who is the listed applicant for TC-1111 TRANSFER PIN?

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

What is the FDA product code for TC-1111 TRANSFER PIN?

The FDA product code for TC-1111 TRANSFER PIN 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 Minimatic Implant Technology 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 34 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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