Instrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse

Device Code: 4102

Product Code(s): PWK

Definition: Used To Aid In Insertion, Placement, Fixation, Or Anchoring Of Surgical Mesh For Transabdominal Pelvic Organ Prolapse Repair

Device Classification Information

Device Type ID4102
Device NameInstrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse
Physical StateNeedle Passers And Trocars, Needle Guides, Fixation Tools, And Tissue Anchors Used With Surgical Mesh.
Technical MethodUsed With Urogynecologic Surgical Mesh Instrumentation To Facilitate Transabdominal Pelvic Organ Prolapse Repair Procedures
Target AreaVagina, Uterus, Sacrum, Pelvic Floor
Regulation DescriptionSpecialized Surgical Instrumentation For Use With Urogynecologic Surgical Mesh.
Regulation Medical SpecialtyObstetrics/Gynecology
Review PanelObstetrics/Gynecology
Premarket Review Office Of Device Evaluation (ODE)
Division Of Reproductive, Gastro-Renal, And Urological Devices (DRGUD)
Obstetrics And Gynecology Devices Branch (OGDB)
Submission Type510(k)
CFR Regulation Number884.4910 [🔎]
FDA Device ClassificationClass 2 Medical Device
Product CodePWK
GMP ExemptNo
Summary MRIneligible
Implanted DeviceNo
Life Support DeviceNo
Third Party Review Not Third Party Eligible

Recognized Standards

Total Product Life Cycle

Device Type ID4102
DeviceInstrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse
Product CodePWK
FDA Device ClassificationClass 2 Medical Device
Regulation DescriptionSpecialized Surgical Instrumentation For Use With Urogynecologic Surgical Mesh.
CFR Regulation Number884.4910 [🔎]
Premarket Reviews
ManufacturerDecision
COLOPLAST MANUFACTURING US LLC
 
SUBSTANTIALLY EQUIVALENT
1
TPLC Last Update: 2019-04-02 20:43:02

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