LAMINECTOMY RONGEUR
K-Number: K901372 · 1990-06-28
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Device Summary
Frequently Asked Questions
What is the LAMINECTOMY RONGEUR?
LAMINECTOMY RONGEUR is a medical device that received FDA 510(k) clearance on 1990-06-28. The listed applicant is Zeppelin GmbH. The 510(k) number is K901372.
When did LAMINECTOMY RONGEUR receive FDA 510(k) clearance?
LAMINECTOMY RONGEUR received FDA 510(k) clearance on 1990-06-28, under 510(k) number K901372.
Who is the listed applicant for LAMINECTOMY RONGEUR?
The FDA 510(k) record lists Zeppelin GmbH as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LAMINECTOMY RONGEUR?
The FDA product code for LAMINECTOMY RONGEUR is HAE.
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 Zeppelin GmbH 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: HAE)
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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