Atlas FDA

OBC BONE ANCHORED HEARING SYSTEM

FDA 510(k) clearance K112053 · decided 2011-11-18

Clearance details

K-number
K112053
Device name
OBC BONE ANCHORED HEARING SYSTEM
Applicant
Oticon Medical AB
Decision
Substantially Equivalent
Date received
2011-07-19
Decision date
2011-11-18
Days to decision
122 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
Askim, SE
Third-party review
No
Expedited review
No

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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
BAHA CORDELLE II (K080363)Cochlear Bone Anchored Systems AB2008-04-10
BRANEMARK BONE-ANCHORED HEARING AID (BAHA) SYSTEM FOR PEDIATRIC USE (K984162)Nobelpharma USA, Inc.1999-06-28

Recalls involving this device

No recalls on record reference this clearance.