The following data is part of a premarket notification filed by Orthocon, Inc. with the FDA for Orthocon Absorbable Hemostatic Bone Putty.
| Device ID | K122156 |
| 510k Number | K122156 |
| Device Name: | ORTHOCON ABSORBABLE HEMOSTATIC BONE PUTTY |
| Classification | Wax, Bone |
| Applicant | ORTHOCON, INC. 1 Bridge St Ste 121 Irvington, NY 10533 |
| Contact | Richard Kronenthal |
| Correspondent | Richard Kronenthal ORTHOCON, INC. 1 Bridge St Ste 121 Irvington, NY 10533 |
| Product Code | MTJ |
| CFR Regulation Number | 510(k) Premarket Notification [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-07-20 |
| Decision Date | 2013-01-28 |
| Summary: | summary |