ADJUSTABLE ANGLE GUIDE
K-Number: K903247 · 1990-07-30
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Device Summary
Frequently Asked Questions
What is the ADJUSTABLE ANGLE GUIDE?
ADJUSTABLE ANGLE GUIDE is a medical device that received FDA 510(k) clearance on 1990-07-30. The listed applicant is Onyx Medical Corp.. The 510(k) number is K903247.
When did ADJUSTABLE ANGLE GUIDE receive FDA 510(k) clearance?
ADJUSTABLE ANGLE GUIDE received FDA 510(k) clearance on 1990-07-30, under 510(k) number K903247.
Who is the listed applicant for ADJUSTABLE ANGLE GUIDE?
The FDA 510(k) record lists Onyx Medical Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ADJUSTABLE ANGLE GUIDE?
The FDA product code for ADJUSTABLE ANGLE GUIDE is LXH.
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 Onyx Medical Corp. 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: LXH)
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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