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Single Use Perpos Pls System, 4.5 Bone-Lok Pls Implant
FDA 510(k)U (US FDA 510(k))
510(k) K082795
Identifiers
- 510(k) Number
- K082795 FDA 510(k)
- FDA Product Code
- MRW FDA 510(k)
Classification
- Device Class
- U FDA 510(k)
- Advisory Committee
- Unknown FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Single Use Perpos Pls System, 4.5 Bone-Lok Pls Implant by Interventional Spine, Inc — U — FDA_510K — listed in FDA 510(k) — regulatory data on deviCERTS
Authorization Coverage (1 country)
Regulatory Authorizations
United States Active
FDA_510K
| Source | Region | Type | Cert / Approval No. | Class | Status |
|---|---|---|---|---|---|
| FDA 510(k) | United States | FDA_510K | K082795 | U | Active |
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Manufacturer
- Manufacturer
- Interventional Spine, Inc
- FDA Applicant
- Interventional Spine, Inc.
Sources (1)
- FDA 510(k) K082795 24 fields · synced Jun 19, 2026