VERTEBRAL ACCESS SYSTEM BY VIDACARE
FDA 510(k) clearance K081713 · decided 2008-11-21
Clearance details
- K-number
- K081713
- Device name
- VERTEBRAL ACCESS SYSTEM BY VIDACARE
- Applicant
- Vidacare Corporation
- Decision
- Substantially Equivalent
- Date received
- 2008-06-17
- Decision date
- 2008-11-21
- Days to decision
- 157 days
- Clearance type
- Traditional
- Product code
- MOQ
- Device class
- 1
- Regulation number
- 878.4820
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Irvine, CA, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| NORDIX INC RECHARGEABLE BATTERY PART NUMBER 2116 (K013133) | Nordix, Inc. | 2001-11-13 |
| ALEXANDER MANUFACTURING CO. RECHARGEABLE BATTERY PART NUMBER MS822 (K980224) | Alexander Mfg. Co. | 1998-04-02 |
Recalls involving this device
No recalls on record reference this clearance.