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FDA 510(k)

BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS

K-Number: K070533 · 2007-06-21

ApplicantB.T.I. Biotechnology Institute, Sl.
Decision Date2007-06-21
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is B.T.I. Biotechnology Institute, Sl.. It received FDA 510(k) clearance on 2007-06-21 under 510(k) number K070533. The device is classified under product code NHA. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS?

BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS is a medical device that received FDA 510(k) clearance on 2007-06-21. The listed applicant is B.T.I. Biotechnology Institute, Sl.. The 510(k) number is K070533.

When did BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS receive FDA 510(k) clearance?

BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS received FDA 510(k) clearance on 2007-06-21, under 510(k) number K070533.

Who is the listed applicant for BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS?

The FDA 510(k) record lists B.T.I. Biotechnology Institute, Sl. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS?

The FDA product code for BTI ENDOSSEOUS DENTAL IMPLANT ANGLED ABUTMENTS is NHA.

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Other records listing B.T.I. Biotechnology Institute, Sl. as applicant

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Related Devices (Code: NHA)

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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