The following data is part of a premarket notification filed by K2m, Inc. with the FDA for Range Spinal System.
Device ID | K131784 |
510k Number | K131784 |
Device Name: | RANGE SPINAL SYSTEM |
Classification | Pedicle Screw Spinal System, Adolescent Idiopathic Scoliosis |
Applicant | K2M, INC. 751 MILLER DR.,SE Leesburg, VA 20175 |
Contact | Nancy Giezen |
Correspondent | Nancy Giezen K2M, INC. 751 MILLER DR.,SE Leesburg, VA 20175 |
Product Code | OSH |
Subsequent Product Code | KWP |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3070 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-18 |
Decision Date | 2013-08-30 |
Summary: | summary |