The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Titanium Intramedullary Nail, Titanium Locking Screw.
Device ID | K981529 |
510k Number | K981529 |
Device Name: | TITANIUM INTRAMEDULLARY NAIL, TITANIUM LOCKING SCREW |
Classification | Nail, Fixation, Bone |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | Joann Kuhne |
Correspondent | Joann Kuhne SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | JDS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-04-29 |
Decision Date | 1998-07-09 |
Summary: | summary |