FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

MECTALIF

K Number: K110927 · Decision Jun 13, 2011
Classifications
1
FEI Numbers
418
Registration Numbers
418
Same Product Code
890
Applicant Total
39
Review Days
77

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Basic Information

Device Name
MECTALIF
K Number
K110927
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 28, 2011
Decision Date
June 13, 2011
Product Code
MAX
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
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Similar 510(k) Clearances

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Other Clearances by Medacta International

K Number Device Name
K160605 MectaLIF Anterior Stand-Alone
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
Search all 39 clearances from Medacta International →