The following data is part of a premarket notification filed by Scandius Biomedical, Inc. with the FDA for Scandius Absorbable Acl Reconstruction System.
| Device ID | K041961 |
| 510k Number | K041961 |
| Device Name: | SCANDIUS ABSORBABLE ACL RECONSTRUCTION SYSTEM |
| Classification | Screw, Fixation, Bone |
| Applicant | SCANDIUS BIOMEDICAL, INC. 11A BEAVER BROOK ROAD Littleton, MA 01460 |
| Contact | Eric Bannon |
| Correspondent | Eric Bannon SCANDIUS BIOMEDICAL, INC. 11A BEAVER BROOK ROAD Littleton, MA 01460 |
| Product Code | HWC |
| CFR Regulation Number | 888.3040 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-07-21 |
| Decision Date | 2004-10-20 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 10884521513549 | K041961 | 000 |
| 10884521513310 | K041961 | 000 |
| 10884521513303 | K041961 | 000 |
| 10884521513297 | K041961 | 000 |