# Effective Date of Requirement for Premarket Approval for Surgical Mesh for Transvaginal Pelvic Organ Prolapse Repair
> **Food and Drug Administration** · Final order. · Published 2016-01-05 · Effective 2016-01-05 · 81 FR 364
## Document
- **Document number:** 2015-33163
- **Category:** fda-device
- **Sub-agency:** Food and Drug Administration
- **Federal Register citation:** 81 FR 364
- **CFR reference:** 21 CFR 884
- **Publication date:** 2016-01-05
- **Effective date:** 2016-01-05
- **HHS docket:** Docket No. FDA-2014-N-0298
## Abstract

The Food and Drug Administration (FDA or the Agency) is issuing a final order to require the filing of a premarket approval application (PMA) or notice of completion of a product development protocol (PDP) for surgical mesh for transvaginal pelvic organ prolapse (POP) repair.

## Source
- [Federal Register document](https://www.federalregister.gov/documents/2016/01/05/2015-33163/effective-date-of-requirement-for-premarket-approval-for-surgical-mesh-for-transvaginal-pelvic-organ)
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