The following data is part of a premarket notification filed by Downs Surgical Ltd. with the FDA for Shepperd Nerve Root Retractor W/suction & Fibre.
Device ID | K900615 |
510k Number | K900615 |
Device Name: | SHEPPERD NERVE ROOT RETRACTOR W/SUCTION & FIBRE |
Classification | Arthroscope |
Applicant | DOWNS SURGICAL LTD. PARKWAY CLOSE,PARKWAY INDUSTRIAL ESTATE Sheffield S9 4wj, GB |
Contact | J Newson |
Correspondent | J Newson DOWNS SURGICAL LTD. PARKWAY CLOSE,PARKWAY INDUSTRIAL ESTATE Sheffield S9 4wj, GB |
Product Code | HRX |
CFR Regulation Number | 888.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-02-08 |
Decision Date | 1990-10-22 |