THORTON TITANIUM HOOK ANGLED RIGHT
K-Number: K863988 · 1986-10-31
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Device Summary
Frequently Asked Questions
What is the THORTON TITANIUM HOOK ANGLED RIGHT?
THORTON TITANIUM HOOK ANGLED RIGHT is a medical device that received FDA 510(k) clearance on 1986-10-31. The listed applicant is Keeler Instruments, Inc.. The 510(k) number is K863988.
When did THORTON TITANIUM HOOK ANGLED RIGHT receive FDA 510(k) clearance?
THORTON TITANIUM HOOK ANGLED RIGHT received FDA 510(k) clearance on 1986-10-31, under 510(k) number K863988.
Who is the listed applicant for THORTON TITANIUM HOOK ANGLED RIGHT?
The FDA 510(k) record lists Keeler Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for THORTON TITANIUM HOOK ANGLED RIGHT?
The FDA product code for THORTON TITANIUM HOOK ANGLED RIGHT is HNQ.
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 Keeler Instruments, Inc. 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: HNQ)
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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