MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS
K-Number: K072208 · 2007-09-07
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Device Summary
Frequently Asked Questions
What is the MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS?
MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS is a medical device that received FDA 510(k) clearance on 2007-09-07. The listed applicant is Integra LifeSciences Corporation. The 510(k) number is K072208.
When did MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS receive FDA 510(k) clearance?
MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS received FDA 510(k) clearance on 2007-09-07, under 510(k) number K072208.
Who is the listed applicant for MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS?
The FDA 510(k) record lists Integra LifeSciences Corporation as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS?
The FDA product code for MAYFIELD DISPOSABLE AND REUSABLE TITANIUM SKULL PINS is HBL.
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 Integra LifeSciences Corporation 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: HBL)
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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