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

ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS

K Number: K000232 · Decision Feb 25, 2000
Classifications
1
FEI Numbers
315
Registration Numbers
315
Same Product Code
910
Applicant Total
57
Review Days
29

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Basic Information

Device Name
ROTAGLIDE + MODULAR KNEE SYSTEM WITH FIXED MENISCUS
K Number
K000232
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3560
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Corin USA
Date Received
January 27, 2000
Decision Date
February 25, 2000
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

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K192656 Optimized Positioning System (OPS) Insight
K190143 LARS AC Band Device
K190834 Corin Optimized Position System Functional Hip Analysis (OPS FHA)
K183038 Corin Optimized Positioning System (OPS) Plan
K181061 Corin Optimized Positioning System (OPS) Femoral
K152893 Corin Optimized Positioning System (OPS)
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