The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Krd1 Pedicle Screw System.
Device ID | K092420 |
510k Number | K092420 |
Device Name: | KRD1 PEDICLE SCREW SYSTEM |
Classification | Orthosis, Spinal Pedicle Fixation |
Applicant | SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
Contact | John Sullivan |
Correspondent | John Sullivan SPINEFRONTIER, INC. 500 CUMMINGS CENTER, STE. 3500 Beverly, MA 01915 |
Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-08-06 |
Decision Date | 2009-11-19 |
Summary: | summary |