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 |