DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3
K-Number: K014001 · 2003-02-04
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Device Summary
Frequently Asked Questions
What is the DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3?
DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3 is a medical device that received FDA 510(k) clearance on 2003-02-04. The listed applicant is Oral Osteodistraction, L.P.. The 510(k) number is K014001.
When did DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3 receive FDA 510(k) clearance?
DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3 received FDA 510(k) clearance on 2003-02-04, under 510(k) number K014001.
Who is the listed applicant for DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3?
The FDA 510(k) record lists Oral Osteodistraction, L.P. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3?
The FDA product code for DISTRACTION OSTEOGENESIS ROD APPLIANCES, MODELS 1, 2, AND 3 is MQN.
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 Oral Osteodistraction, L.P. 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: MQN)
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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