FDA 510(k) FDA class 2 Substantially Equivalent 🇮🇹 Italy

LimaCorporate Kirschner Wire

K Number: K203475 · Decision Feb 5, 2021
Classifications
1
FEI Numbers
283
Registration Numbers
283
Same Product Code
203
Applicant Total
64
Review Days
72

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Basic Information

Device Name
LimaCorporate Kirschner Wire
K Number
K203475
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Lima Corporate S.P.A.
Date Received
November 25, 2020
Decision Date
February 5, 2021
Product Code
HTY
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
HTY Pin, Fixation, Smooth

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Other Clearances by Lima Corporate S.P.A.

K Number Device Name
K252352 SMR Shoulder System; PRIMA Glenoid System; PRIMA Humeral System
K251718 ArTT Augments and Buttresses and Bone Screws
K243826 SMR Reverse HP Shoulder System
K250980 Physica System (Physica CR Porous Femoral components)
K243615 Physica Porous Femoral Components
K234011 AMF TT Cones
K233712 PRIMA Humeral System; PRIMA TT Glenoid
K231099 SMR Hybrid Glenoid System
K231925 MINIMA S System
K221758 SMR Stemless Anatomic
Search all 64 clearances from Lima Corporate S.P.A. →