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

CFN-CANNULATED FEMUR NAIL, CTN-CANNULATED TIBIA NAIL, CHN-CANNULATED HUMERAL NAIL

K Number: K132945 · Decision Mar 7, 2014
Classifications
1
FEI Numbers
302
Registration Numbers
302
Same Product Code
528
Applicant Total
8
Review Days
169

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Basic Information

Device Name
CFN-CANNULATED FEMUR NAIL, CTN-CANNULATED TIBIA NAIL, CHN-CANNULATED HUMERAL NAIL
K Number
K132945
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3020
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
I.T.S. GmbH
Date Received
September 19, 2013
Decision Date
March 7, 2014
Product Code
HSB
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
HSB Rod, Fixation, Intramedullary And Accessories

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K260054 I.T.S. PRS Phoenix II
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K210935 I.T.S. Pelvic Reconstruction System (PRS RX & PRS Phoenix)
K142418 I.T.S. Hand Locking Plates System - HLS
K131722 I.T.S. EXTREMITY FIXATION SYSTEMS
K130008 DISTAL ULNA LOCKING PLATE (DUL), ULNA OSTEOTOMY LOCKING PLATE (UOL), 3.0 CANCELLOUS LOCKING SCREW, 3.0 CORTICAL LOCKING