The following data is part of a premarket notification filed by Sodem Diffusion Sa with the FDA for Sodem High Speed System For Neurosurgery & Median Styernotomy.
Device ID | K955174 |
510k Number | K955174 |
Device Name: | SODEM HIGH SPEED SYSTEM FOR NEUROSURGERY & MEDIAN STYERNOTOMY |
Classification | Motor, Surgical Instrument, Pneumatic Powered |
Applicant | SODEM DIFFUSION SA 49 PLAIN ST. North Attleboro, MA 02760 |
Contact | Rosina Robinson |
Correspondent | Rosina Robinson SODEM DIFFUSION SA 49 PLAIN ST. North Attleboro, MA 02760 |
Product Code | GET |
CFR Regulation Number | 878.4820 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1995-11-13 |
Decision Date | 1996-01-22 |