KT2000 KNEE LIGAMENT ARTHROMETER
FDA 510(k) clearance K942059 · decided 1994-09-20
Clearance details
- K-number
- K942059
- Device name
- KT2000 KNEE LIGAMENT ARTHROMETER
- Applicant
- Medmetric Corp.
- Decision
- Substantially Equivalent
- Date received
- 1994-04-29
- Decision date
- 1994-09-20
- Days to decision
- 144 days
- Clearance type
- Traditional
- Product code
- LYH
- Device class
- 1
- Regulation number
- 890.1615
- Medical specialty
- Physical Medicine
- Advisory committee
- Physical Medicine
- Location
- San Diego, 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 |
|---|---|---|
| KT1000/S KNEE LIGAMENT ARTHROMETER (K943197) | Medmetric Corp. | 1995-03-02 |
| DYNAMIC CRUCIATE TESTER (K881876) | Dyonics, Inc. | 1988-11-17 |
| GENUCOM (K834462) | Far Orthopedics, Inc. | 1984-02-09 |
| KT-1000 DEVICE (K812806) | Medmetric Corp. | 1981-11-10 |
Recalls involving this device
No recalls on record reference this clearance.