The following data is part of a premarket notification filed by Ascension Orthopedics, Inc. with the FDA for Ascension Cannulated Screw System.
Device ID | K092440 |
510k Number | K092440 |
Device Name: | ASCENSION CANNULATED SCREW SYSTEM |
Classification | Screw, Fixation, Bone |
Applicant | ASCENSION ORTHOPEDICS, INC. 8700 CAMERON RD., STE. 100 Austin, TX 78754 -3832 |
Contact | Debbie Stearns |
Correspondent | Debbie Stearns ASCENSION ORTHOPEDICS, INC. 8700 CAMERON RD., STE. 100 Austin, TX 78754 -3832 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-08-10 |
Decision Date | 2009-11-05 |
Summary: | summary |