FEMORAL CEMENT REMOVAL INSTRUMENT
FDA 510(k) clearance K840735 · decided 1984-05-14
Clearance details
- K-number
- K840735
- Device name
- FEMORAL CEMENT REMOVAL INSTRUMENT
- Applicant
- Amtech Scientific, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1984-02-21
- Decision date
- 1984-05-14
- Days to decision
- 83 days
- Clearance type
- Traditional
- Product code
- HWX
- Device class
- 1
- Regulation number
- 888.4540
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- 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 |
|---|---|---|
| ACROMED BONE SCREW TAP SLEEVES (K873067) | Buckman Co., Inc. | 1987-09-02 |
Recalls involving this device
No recalls on record reference this clearance.