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

NEO CR KNEE SYSTEM

K Number: K120313 · Decision Apr 20, 2012
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
9
Review Days
79

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Basic Information

Device Name
NEO CR KNEE SYSTEM
K Number
K120313
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Pipeline Orthopedics
Date Received
February 1, 2012
Decision Date
April 20, 2012
Product Code
JWH
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
JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Similar 510(k) Clearances

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

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Other Clearances by Pipeline Orthopedics

K Number Device Name
K131368 NEO KNEE SYSTEM
K132046 PIPELINE KNEE SYSTEM
K130353 PIPELINE TOTAL HIP SYSTEM (LINE EXTENSION)
K131237 PIPELINE TOTAL HIP SYSTEM
K123692 PIPELINE KNEE SYSTEM
K122500 NEO PS KNEE SYSTEM
K113122 PIPELINE CR PRIMARY KNEE SYSTEM
K112802 PIPELINE TOTAL HIP SYSTEM