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

FDA product code PWI · 2 cleared devices

Class 2 Obstetrics/Gynecology
Regulation
21 CFR 884.4910
Review panel
OB
Implant
No
Life sustaining
No
Third party review
No
GMP exempt
No
Clearance span
2017-11-03 – 2018-02-12

Used to aid in insertion, placement, fixation, or anchoring of surgical mesh for transvaginal pelvic organ prolapse repair

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