SYNTHES 90 DEGREE SCREWDRIVER
FDA 510(k) clearance K082649 · decided 2009-04-30
Clearance details
- K-number
- K082649
- Device name
- SYNTHES 90 DEGREE SCREWDRIVER
- Applicant
- Synthes (Usa)
- Decision
- Substantially Equivalent
- Date received
- 2008-09-12
- Decision date
- 2009-04-30
- Days to decision
- 230 days
- Clearance type
- Traditional
- Product code
- DZI
- Device class
- 2
- Regulation number
- 872.4120
- Medical specialty
- Dental
- Advisory committee
- Dental
- Location
- West Chester, PA, US
- Third-party review
- No
- Expedited review
- No
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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 |