The following data is part of a premarket notification filed by Biocomposites Ltd. with the FDA for Little Grafter Screw.
Device ID | K040265 |
510k Number | K040265 |
Device Name: | LITTLE GRAFTER SCREW |
Classification | Screw, Fixation, Bone |
Applicant | BIOCOMPOSITES LTD. ETRUSCAN ST., ETRURIA Stoke On Trent, GB St1 5pq |
Contact | J. Stephen Bratt |
Correspondent | J. Stephen Bratt BIOCOMPOSITES LTD. ETRUSCAN ST., ETRURIA Stoke On Trent, GB St1 5pq |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-02-05 |
Decision Date | 2004-05-28 |
Summary: | summary |