INTRAMEDULLARY SYSTEMS
K-Number: K930972 · 1994-03-29
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Device Summary
Frequently Asked Questions
What is the INTRAMEDULLARY SYSTEMS?
INTRAMEDULLARY SYSTEMS is a medical device that received FDA 510(k) clearance on 1994-03-29. The listed applicant is Baumer Ortopedia , Ltd.. The 510(k) number is K930972.
When did INTRAMEDULLARY SYSTEMS receive FDA 510(k) clearance?
INTRAMEDULLARY SYSTEMS received FDA 510(k) clearance on 1994-03-29, under 510(k) number K930972.
Who is the listed applicant for INTRAMEDULLARY SYSTEMS?
The FDA 510(k) record lists Baumer Ortopedia , Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAMEDULLARY SYSTEMS?
The FDA product code for INTRAMEDULLARY SYSTEMS is HSB.
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 Baumer Ortopedia , Ltd. 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: HSB)
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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