FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

icotec Cervical Cage

K Number: K192897 · Decision Mar 20, 2020
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
16
Review Days
161

Basic Information

Device Name
icotec Cervical Cage
K Number
K192897
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Icotec AG
Date Received
October 11, 2019
Decision Date
March 20, 2020
Product Code
ODP
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
ODP Intervertebral Fusion Device With Bone Graft, Cervical

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Other Clearances by Icotec AG

K Number Device Name
K252327 CMORE® CT System; CMORE® CT System Navigated Instruments
K242900 VADER® Pedicle System and VADER®one Pedicle System
K233215 icotec Anterior Cervical Plate System
K232792 icotec Interbody Cage System (icotec Cervical Cage, icotec PLIF Lumbar Cage, icotec ETurn™ TLIF Lumbar Cage)
K232790 KONG®-TL VBR System and KONG® C VBR System
K232628 VADER® Pedicle System
K230861 VADER® Pedicle System Navigated Instruments
K222789 VADER® Pedicle System, G21 Cement
K201587 icotec Anterior Cervical Plate System
K200596 G21 Cement, VADER® Pedicle System
Search all 16 clearances from Icotec AG →