The following data is part of a premarket notification filed by Sims Surgical, Inc. with the FDA for Neurosurgical Headframe Accessories.
Device ID | K902517 |
510k Number | K902517 |
Device Name: | NEUROSURGICAL HEADFRAME ACCESSORIES |
Classification | Retractor, Self-retaining, For Neurosurgery |
Applicant | SIMS SURGICAL, INC. 15 KIT ST. P.O. BOX 724 Keene, NH 03431 |
Contact | John D Forster |
Correspondent | John D Forster SIMS SURGICAL, INC. 15 KIT ST. P.O. BOX 724 Keene, NH 03431 |
Product Code | GZT |
CFR Regulation Number | 882.4800 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-07 |
Decision Date | 1990-07-03 |