The following data is part of a premarket notification filed by Surgical Navigation Technologies, Inc. with the FDA for Snt Disposable Biopsy Needle.
Device ID | K971247 |
510k Number | K971247 |
Device Name: | SNT DISPOSABLE BIOPSY NEEDLE |
Classification | Neurological Stereotaxic Instrument |
Applicant | SURGICAL NAVIGATION TECHNOLOGIES, INC. 530 COMPTON ST. Broomfield, CO 80020 |
Contact | David A Mire |
Correspondent | David A Mire SURGICAL NAVIGATION TECHNOLOGIES, INC. 530 COMPTON ST. Broomfield, CO 80020 |
Product Code | HAW |
CFR Regulation Number | 882.4560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1997-04-03 |
Decision Date | 1997-06-16 |
Summary: | summary |