← Back to catalogue
Self Retaining Soft Tissue Retractor
FDA 510(k)Class I (US FDA 510(k))
510(k) K101609
Identifiers
- 510(k) Number
- K101609 FDA 510(k)
- FDA Product Code
- LXH FDA 510(k)
Classification
- Device Class
- Class I FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.4540 FDA 510(k)
- Regulation Number
- 888.4540 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Self Retaining Soft Tissue Retractor by Koros USA, Inc. — Class I — 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 | K101609 | Class I | Active |
Is this your device? Claim it to add documentation and request validation.
Manufacturer
- Manufacturer
- Koros USA, Inc.
Sources (1)
- FDA 510(k) K101609 24 fields · synced Jun 18, 2026