The following data is part of a premarket notification filed by Howmedica Corp. with the FDA for Alta Femoral Intramedullary Rod System, Add Sizes.
Device ID | K922266 |
510k Number | K922266 |
Device Name: | ALTA FEMORAL INTRAMEDULLARY ROD SYSTEM, ADD SIZES |
Classification | Rod, Fixation, Intramedullary And Accessories |
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 | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1992-05-08 |
Decision Date | 1992-09-21 |