The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for A.l.p.s. Calcaneal Plating System.
| Device ID | K132898 |
| 510k Number | K132898 |
| Device Name: | A.L.P.S. CALCANEAL PLATING SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
| Contact | Jared Cooper |
| Correspondent | Jared Cooper BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-09-16 |
| Decision Date | 2013-11-19 |
| Summary: | summary |