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FDA 510(k)

INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS

K-Number: K040205 · 2004-03-22

ApplicantIntra-Lock International
Decision Date2004-03-22
Product CodeNHA
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Intra-Lock International. It received FDA 510(k) clearance on 2004-03-22 under 510(k) number K040205. 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 INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS?

INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS is a medical device that received FDA 510(k) clearance on 2004-03-22. The listed applicant is Intra-Lock International. The 510(k) number is K040205.

When did INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS receive FDA 510(k) clearance?

INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS received FDA 510(k) clearance on 2004-03-22, under 510(k) number K040205.

Who is the listed applicant for INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS?

The FDA 510(k) record lists Intra-Lock International as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS?

The FDA product code for INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTS is NHA.

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Other records listing Intra-Lock International 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.

K130140INTRA-LOCK OP DENTAL IMPLANTK080598MINI DRIVE-LOCK DENTAL IMPLANT SYSTEM PROSTHETICSK070601MINI DRIVE-LOCK DENTAL IMPLANT SYSTEMK050970MILO DENTAL IMPLANT SYSTEMK031322INTRA-LOCK HYDROXYAPATITE COATED IMPLANTSK021915TRANSITIONAL IMPLANTS

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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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