The following data is part of a premarket notification filed by Ascension Orthopedics with the FDA for Integra Total Ankle Replacement System.
Device ID | K151459 |
510k Number | K151459 |
Device Name: | Integra Total Ankle Replacement System |
Classification | Prosthesis, Ankle, Semi-constrained, Cemented, Metal/polymer |
Applicant | Ascension Orthopedics 8700 Cameron Road, Suite 100 Austin, TX 78754 |
Contact | Frederic Testa |
Correspondent | Steve Brown CoorsTek Medical 560 W. Golf Course Rd.. Providence, UT 84332 |
Product Code | HSN |
CFR Regulation Number | 888.3110 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-06-01 |
Decision Date | 2015-08-31 |
Summary: | summary |