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

MasterLoc Stem

K Number: K151531 · Decision Oct 30, 2015
Classifications
1
FEI Numbers
276
Registration Numbers
276
Same Product Code
530
Applicant Total
39
Review Days
144

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Basic Information

Device Name
MasterLoc Stem
K Number
K151531
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International
Date Received
June 8, 2015
Decision Date
October 30, 2015
Product Code
LZO
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
LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

Similar 510(k) Clearances

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

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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
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 →