The following data is part of a premarket notification filed by Kirschner Medical Corp. with the FDA for Btm Total Hip System.
Device ID | K852420 |
510k Number | K852420 |
Device Name: | BTM TOTAL HIP SYSTEM |
Classification | Prosthesis, Hip, Hemi-, Femoral, Metal |
Applicant | KIRSCHNER MEDICAL CORP. 9690 DEERECO ROADD Timonium, MD 21093 |
Contact | Sam Son |
Correspondent | Sam Son KIRSCHNER MEDICAL CORP. 9690 DEERECO ROADD Timonium, MD 21093 |
Product Code | KWL |
CFR Regulation Number | 888.3360 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1985-06-07 |
Decision Date | 1985-06-28 |