WRENCH
FDA 510(k) clearance K791073 · decided 1979-06-20
Clearance details
- K-number
- K791073
- Device name
- WRENCH
- Applicant
- Truth, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-06-12
- Decision date
- 1979-06-20
- Days to decision
- 8 days
- Clearance type
- Traditional
- Product code
- HXC
- Device class
- 1
- Regulation number
- 888.4540
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Mchenry, IL, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Truth
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| Intellitorq (K180092) | Gauthier Biomedical, Inc. | 2018-03-08 |
| ADJUSTABLE WRENCHES (K874359) | Med-Tool, Inc. | 1987-11-23 |
| COMBINATION WRENCHES (K874358) | Med-Tool, Inc. | 1987-11-23 |
| TORQUEDRIVER WRENCH (K870053) | Jerome Medical | 1987-03-11 |
| SPINAL WRENCH (K813067) | Twin City Surgical, Inc. | 1981-11-24 |
Recalls involving this device
No recalls on record reference this clearance.