Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

IMPLA-MED TITANIUM, IMPLANT DEVICES

K-Number: K900061 · 1990-04-27

ApplicantImpla-Med
Decision Date1990-04-27
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLA-MED TITANIUM, IMPLANT DEVICES is the device name listed in this FDA 510(k) record. The listed applicant is Impla-Med. It received FDA 510(k) clearance on 1990-04-27 under 510(k) number K900061. 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 IMPLA-MED TITANIUM, IMPLANT DEVICES?

IMPLA-MED TITANIUM, IMPLANT DEVICES is a medical device that received FDA 510(k) clearance on 1990-04-27. The listed applicant is Impla-Med. The 510(k) number is K900061.

When did IMPLA-MED TITANIUM, IMPLANT DEVICES receive FDA 510(k) clearance?

IMPLA-MED TITANIUM, IMPLANT DEVICES received FDA 510(k) clearance on 1990-04-27, under 510(k) number K900061.

Who is the listed applicant for IMPLA-MED TITANIUM, IMPLANT DEVICES?

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

What is the FDA product code for IMPLA-MED TITANIUM, IMPLANT DEVICES?

The FDA product code for IMPLA-MED TITANIUM, IMPLANT DEVICES 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 Impla-Med 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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑