PATIENT SPECIFIC DISTAL FEMORAL
FDA 510(k) clearance K140898 · decided 2015-01-20
Clearance details
- K-number
- K140898
- Device name
- PATIENT SPECIFIC DISTAL FEMORAL
- Applicant
- Stanmore Implants Worldwide , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 2014-04-08
- Decision date
- 2015-01-20
- Days to decision
- 287 days
- Clearance type
- Special
- Product code
- KRO
- Device class
- 2
- Regulation number
- 888.3510
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Plymouth, MA, US
- Third-party review
- No
- Expedited review
- No
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Recalls involving this device
| Record | Firm | Date |
|---|---|---|
| Short tibial bearing MK4 - Std, STM, Catalog No. SMMLTB02. Knee prosthesis component. recall (Z-1778-2022) | Howmedica Osteonics Corp. | 2022-09-23 |