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FDA 510(k)

FRIALIT-2 PROTECT ABUTMENT

K-Number: K974628 · 1998-03-11

ApplicantFriatec AG
Decision Date1998-03-11
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

FRIALIT-2 PROTECT ABUTMENT is the device name listed in this FDA 510(k) record. The listed applicant is Friatec AG. It received FDA 510(k) clearance on 1998-03-11 under 510(k) number K974628. 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 FRIALIT-2 PROTECT ABUTMENT?

FRIALIT-2 PROTECT ABUTMENT is a medical device that received FDA 510(k) clearance on 1998-03-11. The listed applicant is Friatec AG. The 510(k) number is K974628.

When did FRIALIT-2 PROTECT ABUTMENT receive FDA 510(k) clearance?

FRIALIT-2 PROTECT ABUTMENT received FDA 510(k) clearance on 1998-03-11, under 510(k) number K974628.

Who is the listed applicant for FRIALIT-2 PROTECT ABUTMENT?

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

What is the FDA product code for FRIALIT-2 PROTECT ABUTMENT?

The FDA product code for FRIALIT-2 PROTECT ABUTMENT 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 Friatec AG 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.

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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