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

CORIN TRIFIT TS HIP

K Number: K121563 · Decision Oct 5, 2012
Classifications
1
FEI Numbers
189
Registration Numbers
189
Same Product Code
158
Applicant Total
57
Review Days
129

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Basic Information

Device Name
CORIN TRIFIT TS HIP
K Number
K121563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3353
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Corin USA
Date Received
May 29, 2012
Decision Date
October 5, 2012
Product Code
MEH
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
MEH Prosthesis, Hip, Semi-Constrained, Uncemented, Metal / Polymer, Non-Porous, Calcium Phosphate

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Other Clearances by Corin USA

K Number Device Name
K203751 OMNIVision system
K202805 Optimized Positioning System (OPS) Insight
K193545 Corin Optimized Positioning System (OPS) Femoral
K193042 Optimized Positioning System (OPS) ReView
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)
Search all 57 clearances from Corin USA →