The following data is part of a premarket notification filed by Arthrocare Corp. with the FDA for Arthrocare Cavity Spinewand.
| Device ID | K063172 |
| 510k Number | K063172 |
| Device Name: | ARTHROCARE CAVITY SPINEWAND |
| Classification | Electrosurgical, Cutting & Coagulation & Accessories |
| Applicant | ARTHROCARE CORP. 680 VAQUEROS AVE. Sunnyvale, CA 94085 -3523 |
| Contact | Valerie Defiesta-ng |
| Correspondent | Valerie Defiesta-ng ARTHROCARE CORP. 680 VAQUEROS AVE. Sunnyvale, CA 94085 -3523 |
| Product Code | GEI |
| CFR Regulation Number | 878.4400 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-10-18 |
| Decision Date | 2007-04-27 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00817470004236 | K063172 | 000 |
| 00817470002041 | K063172 | 000 |