INTEROSSEOUS NEEDLE
K-Number: K761206 · 1976-12-13
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Device Summary
Frequently Asked Questions
What is the INTEROSSEOUS NEEDLE?
INTEROSSEOUS NEEDLE is a medical device that received FDA 510(k) clearance on 1976-12-13. The listed applicant is Smith & Nephew, Mpl Division. The 510(k) number is K761206.
When did INTEROSSEOUS NEEDLE receive FDA 510(k) clearance?
INTEROSSEOUS NEEDLE received FDA 510(k) clearance on 1976-12-13, under 510(k) number K761206.
Who is the listed applicant for INTEROSSEOUS NEEDLE?
The FDA 510(k) record lists Smith & Nephew, Mpl Division as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTEROSSEOUS NEEDLE?
The FDA product code for INTEROSSEOUS NEEDLE is DZM.
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 Smith & Nephew, Mpl Division 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: DZM)
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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