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Tryptik Ca Anterior Intersomatic Cervical Cage, Models Mos-Ca 12 05-S, Mos-Ca 1…
FDA 510(k)Class II (US FDA 510(k))
510(k) K091873
by Spineart
Identifiers
- 510(k) Number
- K091873 FDA 510(k)
- FDA Product Code
- ODP FDA 510(k)
Classification
- Device Class
- Class II FDA 510(k)
- Legislation / Framework
- 21 CFR Part 888.3080 FDA 510(k)
- Regulation Number
- 888.3080 FDA 510(k)
- Advisory Committee
- Orthopedic FDA 510(k)
- FDA Decision
- SESE Substantially Equivalent FDA 510(k)
Tryptik Ca Anterior Intersomatic Cervical Cage, Models Mos-Ca 12 05-S, Mos-Ca 1… by Spineart — Class II — FDA_510K — listed in FDA 510(k)
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 | K091873 | Class II | Active |
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Manufacturer
- Manufacturer
- Spineart
Sources (1)
- FDA 510(k) K091873 24 fields · synced Jun 18, 2026