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

MectaLIF Anterior Stand-Alone

K Number: K160605 · Decision Jul 21, 2016
Classifications
1
FEI Numbers
253
Registration Numbers
253
Same Product Code
200
Applicant Total
39
Review Days
141

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Basic Information

Device Name
MectaLIF Anterior Stand-Alone
K Number
K160605
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
March 2, 2016
Decision Date
July 21, 2016
Product Code
OVD
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
OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Similar 510(k) Clearances

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Other Clearances by Medacta International

K Number Device Name
K160289 MasterLoc Stem
K153664 M.U.S.T. Pedicle Screw System
K151531 MasterLoc Stem
K142744 Mecta-C TiPEEK
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
Search all 39 clearances from Medacta International →