ISOLA CLOSED DUAL ROD CONNECTOR
K-Number: K003822 · 2001-01-08
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Device Summary
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.
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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