Cedar Surgical, Inc.
North Oaks, MN, US
Cedar Surgical, Inc. appears in FDA device records in North Oaks, MN. FDA records list 17 510(k) clearances between and , no PMA records and no registered establishments. As of , FDA records show no recalls for this company.
FDA records held for this company
- 510(k) clearances
- 17
- PMA records
- 0
- Recall records
- 0
- Registered establishments
- 0
510(k) clearance history
FDA records hold 17 510(k) clearances for Cedar Surgical, Inc. between 1985 and 1987. The busiest year on record is 1986, with 8. The most recent is 1987, with 4.
Clearances by year, as a table
| Year | Clearances |
|---|---|
| 1985 | 5 |
| 1986 | 8 |
| 1987 | 4 |
| K number | Device | Product code | Decision | Decision date |
|---|---|---|---|---|
| K873692 | RAYLOR(TM) DRILL STOP | HBE | Substantially Equivalent | |
| K872281 | RAYLOR FUSION FUNNEL | HXR | Substantially Equivalent | |
| K873690 | CEDAR(TM) PELVIC CUSHION | LWG | Substantially Equivalent | |
| K873691 | CEDAR(TM) RETRACTOR RING | GZT | Substantially Equivalent | |
| K864425 | RAYLOR(TM) DISSECTING HOOK | GDG | Substantially Equivalent | |
| K864426 | RAYLOR(TM) DEPTH GAUGE | HTJ | Substantially Equivalent | |
| K864424 | RAYLOR(TM) PROTECTIVE RETRACTOR | GAD | Substantially Equivalent | |
| K864421 | RAYLOR(TM) PERIOSTEAL ELEVATORS | GEG | Substantially Equivalent | |
| K864423 | RAYLOR(TM) OSTEOTOMES | Substantially Equivalent | ||
| K864422 | RAYLOR(TM) MALLET | HWA | Substantially Equivalent | |
| K863416 | RAYLOR MINI-PROBE | HAO | Substantially Equivalent | |
| K863415 | RAYLOR BONE IMPACTORS | HAO | Substantially Equivalent | |
| K853800 | UPPER-CHEST-SUPPORT CUSHION FOR OPERATIONS IN SITT | Substantially Equivalent | ||
| K853799 | NEUROSURGICAL HEADREST | Substantially Equivalent | ||
| K853798 | BONE IMPACTORS | Substantially Equivalent | ||
| K853797 | KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR | Substantially Equivalent | ||
| K853796 | RAYLOR RETRACTORS | GAD | Substantially Equivalent |
Registered establishments
No FDA establishment registrations recorded against this company.
FDA product codes
- HBEDrills, Burrs, Trephines & Accessories (Simple, Powered)
- GEGElevator, Surgical, General & Plastic Surgery
- HTJGauge, Depth
- GDGHook, Surgical, General & Plastic Surgery
- HWAImpactor
- HAOInstrument, Surgical, Non-Powered
- GADRetractor
- GZTRetractor, Self-Retaining, For Neurosurgery
- HXRSpatula, Orthopedic
- LWGSurgical Table Cushion
Recall records
No recall records for this company in the ingested FDA data.
Verification record
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Data as of , FDA export datePage updated Source: openFDA, public domain