ACROMED BONE PLATE BENDER
FDA 510(k) clearance K872949 · decided 1987-10-15
Clearance details
- K-number
- K872949
- Device name
- ACROMED BONE PLATE BENDER
- Applicant
- Buckman Co., Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-07-28
- Decision date
- 1987-10-15
- Days to decision
- 79 days
- Clearance type
- Traditional
- Product code
- HXW
- Device class
- 1
- Regulation number
- 888.4540
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Martinez, 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 |
|---|---|---|
| DRIVER-BENDER-EXTRACTOR, BONE PIN (K870668) | Military Engineering, Inc. | 1987-03-09 |
| RD 140 SURGICAL BENDER (K870084) | Terray Manufacturing, Inc. | 1987-01-28 |
Recalls involving this device
No recalls on record reference this clearance.