The following data is part of a premarket notification filed by Steri-oss, Inc. with the FDA for Bone Cutting Instrument And Accessories.
| Device ID | K950936 |
| 510k Number | K950936 |
| Device Name: | BONE CUTTING INSTRUMENT AND ACCESSORIES |
| Classification | Implant, Endosseous, Root-form |
| Applicant | STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
| Contact | Paul Gasser |
| Correspondent | Paul Gasser STERI-OSS, INC. 22895 EASTPARK DR. Yorba Linda, CA 92887 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1995-03-01 |
| Decision Date | 1995-04-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 07332747091045 | K950936 | 000 |
| 07332747091038 | K950936 | 000 |
| 07332747091021 | K950936 | 000 |
| 07332747091014 | K950936 | 000 |
| 07332747091007 | K950936 | 000 |
| 07332747083828 | K950936 | 000 |