KEY DRILL
FDA 510(k) clearance K821127 · decided 1982-06-03
Clearance details
- K-number
- K821127
- Device name
- KEY DRILL
- Applicant
- Key Medical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1982-04-20
- Decision date
- 1982-06-03
- Days to decision
- 44 days
- Clearance type
- Traditional
- Product code
- GFG
- Device class
- 1
- Regulation number
- 878.4820
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Mchenry, IL, 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 |
|---|---|---|
| MITEK MODULAR DRILL BIT (K935225) | Mitek Surgical Products, Inc. | 1994-04-07 |
| MICRO DRILLS (K821486) | Spire Medical, Inc. | 1982-06-09 |
Recalls involving this device
No recalls on record reference this clearance.