CEDAR(TM) PELVIC CUSHION
FDA 510(k) clearance K873690 · decided 1987-10-26
Clearance details
- K-number
- K873690
- Device name
- CEDAR(TM) PELVIC CUSHION
- Applicant
- Cedar Surgical, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1987-09-08
- Decision date
- 1987-10-26
- Days to decision
- 48 days
- Clearance type
- Traditional
- Product code
- LWG
- Device class
- 1
- Regulation number
- 878.4950
- Medical specialty
- General, Plastic Surgery
- Advisory committee
- General, Plastic Surgery
- Location
- Minnetonka, MN, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Cedar Surgical
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| CHOP SPINE FRAME (K883295) | Avec Scientific Design Corp. | 1988-08-23 |
| SHOULDER BOLSTER, KNEE, ANKLE & LEG SUPPORT PADS (K882520) | Karlin Technology, Inc. | 1988-07-18 |
| KAMBIN LAMINECTOMY FRAME (K874494) | Avec Scientific Design Corp. | 1987-11-23 |
Recalls involving this device
No recalls on record reference this clearance.