MOBI-C Cervical Disc Prosthesis
FDA premarket approval P110009/S019 · decided 2017-06-02
Approval details
- PMA number
- P110009
- Supplement
- S019
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- MOBI-C Cervical Disc Prosthesis
- Generic name
- Prosthesis, intervertebral disc
- Applicant
- Highridge Medical, LLC
- Date received
- 2017-05-05
- Decision date
- 2017-06-02
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MJO
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Westminister, CO
- Statement
- Manufacturing changes that include the addition of a new plasma spray coating supplier and raw titanium material supplier
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| Vital™ Spinal Fixation System (K253093) | Highridge Medical, LLC | 2025-12-17 |
| Virage® OCT Spinal Fixation System (K250332) | Highridge Medical, LLC | 2025-04-04 |