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

CLIPLOC SOFT TISSUE MARKER 18G/100MM (4), /130MM (5 1/8), /150MM (6), MODELS 12370, 12372, 12376

K Number: K033447 · Decision Jan 28, 2004
Classifications
1
FEI Numbers
102
Registration Numbers
102
Same Product Code
109
Applicant Total
71
Review Days
91

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Basic Information

Device Name
CLIPLOC SOFT TISSUE MARKER 18G/100MM (4), /130MM (5 1/8), /150MM (6), MODELS 12370, 12372, 12376
K Number
K033447
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Mri Devices Corp.
Date Received
October 29, 2003
Decision Date
January 28, 2004
Product Code
NEU
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
NEU Marker, Radiographic, Implantable

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Other Clearances by Mri Devices Corp.

K Number Device Name
K041286 DYNACAD V1.0
K041481 MODEL BBC-127 BIOPSY BREAST COIL
K040349 MODIFICATION TO HRW-127 WRIST ARRAY COIL
K040348 MODIFICATION TO HNC-127-INT NEUROVASCULAR ARRAY COIL
K040288 QSC-127-INT SHOULDER ARRAY COIL SET
K033567 MODELS HRK-63-8 PMS AND HRK-127-8 KNEE ARRAY COILS
K032576 BIOPSY BREAST COIL, MODEL BBC
K033151 KFA-12 KNEE, FOOT, AND ANKLE ARRAY COIL
K033152 HAC-12 AND HAC-30 HEAD ARRAY COIL
K032633 HRK-63-8 KNEE ARRAY COIL
Search all 71 clearances from Mri Devices Corp. →