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 |