PLASTER STAND
FDA 510(k) clearance K870100 · decided 1987-01-28
Clearance details
- K-number
- K870100
- Device name
- PLASTER STAND
- Applicant
- Orthopedic Systems, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-01-09
- Decision date
- 1987-01-28
- Days to decision
- 19 days
- Clearance type
- Traditional
- Product code
- LGG
- Device class
- 1
- Regulation number
- 888.5980
- Medical specialty
- Orthopedic
- Advisory committee
- Orthopedic
- Location
- Hayward, 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 |
|---|---|---|
| 27-230 TO 27-234 VARIOUS CAST BREAKERS, WOLF (K851786) | Artiberia | 1985-07-09 |
| MODULAR EXTREMITY CASTING SUPPORT (K834384) | Buckman Co., Inc. | 1984-01-30 |
Recalls involving this device
No recalls on record reference this clearance.