The following data is part of a premarket notification filed by Sofamor Danek Usa,inc. with the FDA for Acpii Anterior Cervical Plate System.
Device ID | K970806 |
510k Number | K970806 |
Device Name: | ACPII ANTERIOR CERVICAL PLATE SYSTEM |
Classification | Appliance, Fixation, Spinal Intervertebral Body |
Applicant | SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Contact | Richard W Treharne |
Correspondent | Richard W Treharne SOFAMOR DANEK USA,INC. 1800 PYRAMID PLACE Memphis, TN 38132 |
Product Code | KWQ |
CFR Regulation Number | 888.3060 [🔎] |
Decision | Substantially Equivalent For Some Indications (SN) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-03-05 |
Decision Date | 1997-05-02 |
Summary: | summary |