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FDA 510(k)

ISOLA CLOSED DUAL ROD CONNECTOR

K-Number: K003822 · 2001-01-08

ApplicantDepuyacromed
Decision Date2001-01-08
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ISOLA CLOSED DUAL ROD CONNECTOR is the device name listed in this FDA 510(k) record. The listed applicant is Depuyacromed. It received FDA 510(k) clearance on 2001-01-08 under 510(k) number K003822. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ISOLA CLOSED DUAL ROD CONNECTOR?

ISOLA CLOSED DUAL ROD CONNECTOR is a medical device that received FDA 510(k) clearance on 2001-01-08. The listed applicant is Depuyacromed. The 510(k) number is K003822.

When did ISOLA CLOSED DUAL ROD CONNECTOR receive FDA 510(k) clearance?

ISOLA CLOSED DUAL ROD CONNECTOR received FDA 510(k) clearance on 2001-01-08, under 510(k) number K003822.

Who is the listed applicant for ISOLA CLOSED DUAL ROD CONNECTOR?

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

What is the FDA product code for ISOLA CLOSED DUAL ROD CONNECTOR?

The FDA product code for ISOLA CLOSED DUAL ROD CONNECTOR is KWP.

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 Depuyacromed 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 48 devices →

Related Devices (Code: KWP)

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.

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