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 |