PERIOGRAF
Bone Grafting Material, Synthetic
STERLING DRUG, INC.
The following data is part of a premarket notification filed by Sterling Drug, Inc. with the FDA for Periograf.
Pre-market Notification Details
| Device ID | K813070 |
| 510k Number | K813070 |
| Device Name: | PERIOGRAF |
| Classification | Bone Grafting Material, Synthetic |
| Applicant | STERLING DRUG, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | LYC |
| CFR Regulation Number | 872.3930 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-11-02 |
| Decision Date | 1981-11-20 |
Trademark Results [PERIOGRAF]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PERIOGRAF 73331033 1227423 Dead/Expired |
Sterling Drug Inc. 1981-10-05 |
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