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)

IMZ INTRAMOBILE CYLINDER IMPLANT

K-Number: K855032 · 1986-03-03

Decision Date1986-03-03
Product CodeDZE
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMZ INTRAMOBILE CYLINDER IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Interpore Intl.. It received FDA 510(k) clearance on 1986-03-03 under 510(k) number K855032. 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 IMZ INTRAMOBILE CYLINDER IMPLANT?

IMZ INTRAMOBILE CYLINDER IMPLANT is a medical device that received FDA 510(k) clearance on 1986-03-03. The listed applicant is Interpore Intl.. The 510(k) number is K855032.

When did IMZ INTRAMOBILE CYLINDER IMPLANT receive FDA 510(k) clearance?

IMZ INTRAMOBILE CYLINDER IMPLANT received FDA 510(k) clearance on 1986-03-03, under 510(k) number K855032.

Who is the listed applicant for IMZ INTRAMOBILE CYLINDER IMPLANT?

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

What is the FDA product code for IMZ INTRAMOBILE CYLINDER IMPLANT?

The FDA product code for IMZ INTRAMOBILE CYLINDER IMPLANT 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 Interpore Intl. 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.

View all 25 devices →

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.

↑