The following data is part of a premarket notification filed by Kyphon, Inc. with the FDA for Kyphx Xpander Inflatable Bone Tamps Model#ko8a,ko9a,k13a.
| Device ID | K041454 |
| 510k Number | K041454 |
| Device Name: | KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13A |
| Classification | Arthroscope |
| Applicant | KYPHON, INC. 1221 CROSSMAN AVE. Sunnyvale, CA 94089 |
| Contact | Cindy Domescus |
| Correspondent | Cindy Domescus KYPHON, INC. 1221 CROSSMAN AVE. Sunnyvale, CA 94089 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-06-01 |
| Decision Date | 2004-07-09 |
| Summary: | summary |