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

CALDERA MESH

K Number: K060004 · Decision Feb 22, 2006
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
335
Applicant Total
22
Review Days
50

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Basic Information

Device Name
CALDERA MESH
K Number
K060004
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.3300
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Caldera Medical, Inc.
Date Received
January 3, 2006
Decision Date
February 22, 2006
Product Code
FTL
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
FTL Mesh, Surgical, Polymeric

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Other Clearances by Caldera Medical, Inc.

K Number Device Name
K233500 Benesta Tissue Removal Device
K211975 Desara TV EZ 3.0 System, Desara Blue TV EZ 3.0 System, Desara TV EZ 2.7 System, Desara Blue TV EZ 2.7 System
K192811 BenestaTM Tissue Removal Device
K192822 Benesta Hysteroscope
K193603 Benesta Medical Sterilization Tray
K191416 Desara One Single Incision Sling System, 1 Pack ; Desara One Single Incision Sling System, 3 Pack
K172614 Caldera Medical Transobturator Helical Introducer, Left; Caldera Medical Transobturator Helical Introducer, Right; Caldera Medical Transobturator Large Helical Introducer, Left; Caldera Medical Transobturator Large Helical Introducer, Right; Caldera Medical Transobturator Inside-Out Introducer, Left
K162201 Desara TV, Desara Blue TV
K150016 Vertessa Lite
K150023 Vertessa Lite Y-Mesh
Search all 22 clearances from Caldera Medical, Inc. →