The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Vecsei Expanding Screw.
Device ID | K892925 |
510k Number | K892925 |
Device Name: | VECSEI EXPANDING SCREW |
Classification | Screw, Fixation, Bone |
Applicant | HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Contact | Robert E Smith |
Correspondent | Robert E Smith HOWMEDICA CORP. 359 VETERANS BLVD. Rutherford, NJ 07070 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-04-21 |
Decision Date | 1989-08-07 |