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FDA 510(k)

BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II

K-Number: K992872 · 1999-11-24

ApplicantEntific Medical Systems, Inc.
Decision Date1999-11-24
Product CodeLXB
Advisory CommitteeEN
DecisionSubstantially Equivalent

Device Summary

BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II is the device name listed in this FDA 510(k) record. The listed applicant is Entific Medical Systems, Inc.. It received FDA 510(k) clearance on 1999-11-24 under 510(k) number K992872. The device is classified under product code LXB. It was reviewed by the EN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II?

BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II is a medical device that received FDA 510(k) clearance on 1999-11-24. The listed applicant is Entific Medical Systems, Inc.. The 510(k) number is K992872.

When did BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II receive FDA 510(k) clearance?

BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II received FDA 510(k) clearance on 1999-11-24, under 510(k) number K992872.

Who is the listed applicant for BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II?

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 BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II?

The FDA product code for BRANEMARK BONE-ANCHORED HEARING AID (BAHA) CORDELLE II 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.

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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.

K042017BAHA DIVINOK021837BRANENMARK BONE-ANCHORED-HEARING AID (BAHA)K011438BILATERAL FITTING OF THE BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM.K002913HEADBAND FOR BAHA

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.

K253431Bone conduction Hearing Aid (BM100, BM300, BM310, SHOKZHEAR BM400, SHOKZ BM400MN, SHOKZHEAR BM410, SHOKZHEAR BM410MN, SHOKZHEAR BM420 and SHOKZHEAR BM420MN)Shokz Health Global LimitedK254296Ossiclear (Ossiclear System)SounductK260452Bone Conduction Hearing Aid (G41157, G41158, G41159, G41160, G42151, G42152, G42153, G42154, G42155, G42156, G42157, G42158, G42159, G42160, G43151, G43152, G43153, G43154, G43155, G43156, G45151, G45152, G45153, G45154, G45155, G45156, G45157, G45158, G45159, G45160, G46151, G46152, G46153, G46154, G46155, G46156, G46157, G46158)Zdeer Technology (Henan) Co., Ltd.K261256Bone Conduction Hearing Aid (XTS-AISW-D1, XTS-AISW-D2, XTS-AISW-D3)Shenzhen Magnet Technology Co., Ltd.K250215Baha 7 Sound Processor; Baha Fitting Software 7 (P2121898); Baha Smart App (iOS) (P1646054); Baha Smart App (Android) (P1646035); Baha SoundBandCochlearK243041contact forte AlphaBhm-Tech Produktionsgesellschaft Mbh

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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