BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)
K-Number: K021837 · 2002-08-30
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Device Summary
Frequently Asked Questions
What is the BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)?
BRANENMARK BONE-ANCHORED-HEARING AID (BAHA) is a medical device that received FDA 510(k) clearance on 2002-08-30. The listed applicant is Entific Medical Systems, Inc.. The 510(k) number is K021837.
When did BRANENMARK BONE-ANCHORED-HEARING AID (BAHA) receive FDA 510(k) clearance?
BRANENMARK BONE-ANCHORED-HEARING AID (BAHA) received FDA 510(k) clearance on 2002-08-30, under 510(k) number K021837.
Who is the listed applicant for BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)?
The FDA 510(k) record lists Entific Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)?
The FDA product code for BRANENMARK BONE-ANCHORED-HEARING AID (BAHA) is LXB.
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 Entific Medical Systems, 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: LXB)
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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