DRILL, CORDLESS SURGICAL
FDA 510(k) clearance K790063 · decided 1979-02-05
Clearance details
- K-number
- K790063
- Device name
- DRILL, CORDLESS SURGICAL
- Applicant
- Richard'S Medical Equip., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1979-01-15
- Decision date
- 1979-02-05
- Days to decision
- 21 days
- Clearance type
- Traditional
- Product code
- KIJ
- 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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| S & S ORTHOPEDIC WIRE DRIVER 701 (K944488) | S & S Orthopedic , Ltd. | 1995-03-02 |
| ARTHREX GRAFT HARVESTING KIT (K941285) | Arthrex, Inc. | 1994-11-14 |
| THE OSTEOMED B POWER SYSTEM AND ACCESSORIES (K933101) | Osteomed Corp. | 1994-11-07 |
| R AND D BATTERY REPLACEMENT (K933337) | R & D Batteries, Inc. | 1994-04-05 |
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Recalls involving this device
No recalls on record reference this clearance.