PMA
P240027: SpineSeal Spine Sealant
FDA PMA · Sealant, dural · Pramand, LLC
Key facts
| PMA number | P240027 |
|---|---|
| Trade name | SpineSeal Spine Sealant |
| Generic name | Sealant, dural |
| Applicant | Pramand, LLC |
| Owner/operator | Pramand LLC |
| Product code | NQR |
| Approval date | Feb 14, 2025 |
| Docket number | 25M-0438 |
| Establishment registration | 3016980830 |
| FEI number | 3016980830 |
At a glance
- 1–9 Supplements
- Sep 11, 2026 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 1–9 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: