The following data is part of a premarket notification filed by G21 S.r.l. with the FDA for Orthosteady G Bone Cement.
| Device ID | K173494 |
| 510k Number | K173494 |
| Device Name: | OrthoSteady G Bone Cement |
| Classification | Bone Cement |
| Applicant | G21 S.r.l. Via Sandro Petrini, 8 San Possidonio, IT 841039 |
| Contact | Filippo Foroni |
| Correspondent | Barry E. Sands Rqmis, Inc. 110 Haverhill Road Suite 526 Amesbury, MA 01913 |
| Product Code | LOD |
| CFR Regulation Number | 888.3027 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | Yes |
| Date Received | 2017-11-13 |
| Decision Date | 2018-03-06 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08058964729026 | K173494 | 000 |
| 08058964728722 | K173494 | 000 |