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FDA 510(k)

TRANSITIONAL IMPLANTS

K-Number: K021915 · 2002-12-19

ApplicantIntra-Lock International
Decision Date2002-12-19
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

TRANSITIONAL IMPLANTS 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 2002-12-19 under 510(k) number K021915. 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 TRANSITIONAL IMPLANTS?

TRANSITIONAL IMPLANTS is a medical device that received FDA 510(k) clearance on 2002-12-19. The listed applicant is Intra-Lock International. The 510(k) number is K021915.

When did TRANSITIONAL IMPLANTS receive FDA 510(k) clearance?

TRANSITIONAL IMPLANTS received FDA 510(k) clearance on 2002-12-19, under 510(k) number K021915.

Who is the listed applicant for TRANSITIONAL IMPLANTS?

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 TRANSITIONAL IMPLANTS?

The FDA product code for TRANSITIONAL IMPLANTS is DZE.

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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 SYSTEMK040205INTRA-LOCK INTERNATIONAL ANGLED PROSTHETIC ABUTMENTSK031322INTRA-LOCK HYDROXYAPATITE COATED IMPLANTS

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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.

K261392TriActive Dental Implant SystemParagon Implant Mfg., LLCK260463ZEROS Dental Implant SystemZeros Co., Ltd.K251188UNIQA® Dental Implants SystemUniqa Dental, Ltd.K251232MegaGen Zygoma Dental Implant SystemMegagen Implant Co., Ltd.K250806Dental Implant SystemA.B. Dental Devices , Ltd.K260006INOSS SystemInosys, Inc.

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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