PMA
P080013: DURASEAL EXACT SPINE SEALANT SYSTEM
FDA PMA · Sealant, dural · Integra LifeSciences Corporation
Key facts
| PMA number | P080013 |
|---|---|
| Trade name | DURASEAL EXACT SPINE SEALANT SYSTEM |
| Generic name | Sealant, dural |
| Applicant | Integra LifeSciences Corporation |
| Owner/operator | Integra LifeSciences Corporation |
| Product code | NQR |
| Approval date | Sep 4, 2009 |
| Docket number | 09M-0485 |
| Notice date | Oct 6, 2009 |
| Establishment registration | 1121308 |
| FEI number | 1121308 |
At a glance
- 10–99 Supplements
- Feb 27, 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- No Withdrawn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: