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

MySpine Pedicle Screw Placement Guides - LP

K Number: K153273 · Decision Jun 29, 2016
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
302
Applicant Total
165
Review Days
230

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Basic Information

Device Name
MySpine Pedicle Screw Placement Guides - LP
K Number
K153273
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Medacta International S.A.
Date Received
November 12, 2015
Decision Date
June 29, 2016
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

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Other Clearances by Medacta International S.A.

K Number Device Name
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K250644 MSS - Monobloc stem
K251043 Mpact 3D Metal Implants Extension – DMLS Technology
K252847 NextAR Hip Platform
K242603 MyPAO SA guides
K250338 MSS - Humeral reverse liners extension
K250450 Coated hip implants
K252225 PowerKnot High Strength Sutures
Search all 165 clearances from Medacta International S.A. →