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

Mecta-C TiPEEK

K Number: K142744 · Decision May 7, 2015
Classifications
1
FEI Numbers
339
Registration Numbers
339
Same Product Code
348
Applicant Total
39
Review Days
225

Basic Information

Device Name
Mecta-C TiPEEK
K Number
K142744
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3080
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International
Date Received
September 24, 2014
Decision Date
May 7, 2015
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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K Number Device Name
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K143453 Mpact Double Mobility System
K142069 GMK EXTENSION
K141988 M.U.S.T PEDICLE SCREW SYSTEM
K141044 M.U.S.T. EXTENSION
K140826 GMK SPHERE EXTENSION
K140361 META-C CERVICAL PLATE
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