Atlas FDA

BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE

FDA 510(k) clearance K984162 · decided 1999-06-28

Clearance details

K-number
K984162
Device name
BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE
Applicant
Nobelpharma USA, Inc.
Decision
Substantially Equivalent
Date received
1998-11-19
Decision date
1999-06-28
Days to decision
221 days
Clearance type
Traditional
Product code
MAH
Device class
2
Regulation number
874.3302
Medical specialty
Ear, Nose, Throat
Advisory committee
Ear, Nose, Throat
Location
Westmont, IL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
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BA400 14mm Abutment (K150555)Cochlear Americas2015-07-15
Ponto Bone Anchored Hearing system/ Abutment, 14mm. Ponto Bone Anchored Hearing System / Wide implant, 4mm, with abutment, 14 mm (K142678)Oticon Medical AB2015-01-21
COCHLEAR BAHA IMPLANT SYSTEM (K121317)Cochlear Americas2012-10-12
PONTO BONE ANCHORED HEARING SYSTEM (K121228)Oticon Medical AB2012-09-07
OBC BONE ANCHORED HEARING SYSTEM (K112053)Oticon Medical AB2011-11-18
BAHA CORDELLE II (K080363)Cochlear Bone Anchored Systems AB2008-04-10

Recalls involving this device

No recalls on record reference this clearance.