MODIFICATION TO SYNTHES CERVIFIX SYSTEM
FDA 510(k) clearance K030377 · decided 2003-03-06
Clearance details
- K-number
- K030377
- Device name
- MODIFICATION TO SYNTHES CERVIFIX SYSTEM
- Applicant
- Synthes (Usa)
- Decision
- Substantially Equivalent
- Date received
- 2003-02-05
- Decision date
- 2003-03-06
- Days to decision
- 29 days
- Clearance type
- Special
- Product code
- MNI
- Device class
- 2
- Regulation number
- 888.3070
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Paoli, PA, US
- Third-party review
- No
- Expedited review
- No
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| WASTON General Spinal System (K150684) | Changzhou Waston Medical Appliance Co., Ltd. | 2015-11-18 |
| X-spine Pedicle Screw System (K152132) | X-Spine Systems, Inc. | 2015-09-25 |
| Gemmed pedicle screw spinal system (K151592) | Suzhou Gemmed Medical Instrument Co., Ltd. | 2015-09-24 |
Recalls involving this device
No recalls on record reference this clearance.
PMA approvals by this applicant
| Record | Firm | Date |
|---|---|---|
| NORIAN SRS BONE CEMENT (P970010/S004) | Synthes (Usa) | 2000-08-31 |
| NORIAN SRS CEMENT (P970010/S002) | Synthes (Usa) | 2000-04-28 |
| NORIAN SRS CEMENT (P970010/S001) | Synthes (Usa) | 1999-07-16 |
| NORIAN SKELETAL REPAIR SYSTEM (SRS) CANCELLOUS BONE CEMENT (P970010) | Synthes (Usa) | 1998-12-23 |