BRAINLAB HEADPINS
K-Number: K954789 · 1996-08-12
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Device Summary
Frequently Asked Questions
What is the BRAINLAB HEADPINS?
BRAINLAB HEADPINS is a medical device that received FDA 510(k) clearance on 1996-08-12. The listed applicant is Brainlab AG. The 510(k) number is K954789.
When did BRAINLAB HEADPINS receive FDA 510(k) clearance?
BRAINLAB HEADPINS received FDA 510(k) clearance on 1996-08-12, under 510(k) number K954789.
Who is the listed applicant for BRAINLAB HEADPINS?
The FDA 510(k) record lists Brainlab AG as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRAINLAB HEADPINS?
The FDA product code for BRAINLAB HEADPINS is HAW.
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 Brainlab AG 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: HAW)
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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