The following data is part of a premarket notification filed by Encore Medical, L.p with the FDA for Altivate Anatomic Shoulder System.
| Device ID | K162024 |
| 510k Number | K162024 |
| Device Name: | AltiVate Anatomic Shoulder System |
| Classification | Prosthesis, Shoulder, Semi-constrained, Metal/polymer Cemented |
| Applicant | ENCORE MEDICAL, L.P 9800 METRIC BLVD. Austin, TX 78758 |
| Contact | Desiree Wells |
| Correspondent | Desiree Wells ENCORE MEDICAL, L.P 9800 METRIC BLVD. Austin, TX 78758 |
| Product Code | KWS |
| Subsequent Product Code | HSD |
| Subsequent Product Code | PAO |
| CFR Regulation Number | 888.3660 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2016-07-22 |
| Decision Date | 2016-11-21 |
| Summary: | summary |