The following data is part of a premarket notification filed by Link America, Inc. with the FDA for Link Small Bone Plates.
Device ID | K854825 |
510k Number | K854825 |
Device Name: | LINK SMALL BONE PLATES |
Classification | Plate, Fixation, Bone |
Applicant | LINK AMERICA, INC. C/O SURGICAL IMPLANTS, INC. 10 GREAT MEADOW LANE East Hanavor, NJ 07936 |
Contact | Edward B Schussler |
Correspondent | Edward B Schussler LINK AMERICA, INC. C/O SURGICAL IMPLANTS, INC. 10 GREAT MEADOW LANE East Hanavor, NJ 07936 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-12-03 |
Decision Date | 1986-01-21 |