PWK
2018-02-09
Instrumentation, Surgical Mesh, Urogynecologic, Transabdominal Repair Of Pelvic Organ Prolapse
FDA product code PWK · 1 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
- 2018-02-09 – 2018-02-09
Used to aid in insertion, placement, fixation, or anchoring of surgical mesh for transabdominal pelvic organ prolapse repair
No matching devices.
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