Centinel Spine, Inc. · Class II · Cleared May 8, 2018
| K-number | K173347 |
| Device name | STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX |
| Applicant | Centinel Spine, Inc. |
| Product code | MAX |
| Device class | Class II |
| Decision date | May 8, 2018 |
| Decision | Substantially Equivalent |
| Regulation | 888.3080 |
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