The following data is part of a premarket notification filed by Howmedica, Inc. with the FDA for Howmedica(r) Fully Threaded Screws.
Device ID | K974720 |
510k Number | K974720 |
Device Name: | HOWMEDICA(R) FULLY THREADED SCREWS |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | HOWMEDICA, INC. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Contact | Vivian Kelly |
Correspondent | Vivian Kelly HOWMEDICA, INC. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-12-18 |
Decision Date | 1998-03-13 |
Summary: | summary |