FDA 510(k) FDA class 2 Substantially Equivalent 🇦🇹 Austria

BONEBRIDGE System, SAMBA 2 BB, SYMFIT 8.0, SAMBA 2 GO, SAMBA 2 Remote

K Number: K200504 · Decision Jul 29, 2020
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
10
Applicant Total
6
Review Days
149

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
BONEBRIDGE System, SAMBA 2 BB, SYMFIT 8.0, SAMBA 2 GO, SAMBA 2 Remote
K Number
K200504
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.3340
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Med-El Elektromedizinische Geraete GmbH
Date Received
March 2, 2020
Decision Date
July 29, 2020
Product Code
PFO
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
PFO Active Implantable Bone Conduction Hearing System

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (PFO), ordered by most recent decision date.

View all

Other Clearances by Med-El Elektromedizinische Geraete GmbH

K Number Device Name
K201983 BCI 602 Lifts (1 mm), BCI Lifts (1 mm), BCI Lifts (2 mm & 3 mm), BCI Lifts (4 mm)
K191457 BONEBRIDGE System, Bone Conduction Implant Kit (BCI 602 Implant Kit), BCI 602 Sizer Kit, BCI 602 Lifts (1mm)
K183373 Bonebridge
DEN170009 Bonebridge
K172460 ADHEAR System