The following data is part of a premarket notification filed by Peters Surgical with the FDA for Optime, Sinusorb Pga.
| Device ID | K062366 |
| 510k Number | K062366 |
| Device Name: | OPTIME, SINUSORB PGA |
| Classification | Suture, Absorbable, Synthetic, Polyglycolic Acid |
| Applicant | PETERS SURGICAL 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
| Contact | Annie Lasserre |
| Correspondent | Annie Lasserre PETERS SURGICAL 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
| Product Code | GAM |
| CFR Regulation Number | 878.4493 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2006-08-14 |
| Decision Date | 2006-10-02 |
| Summary: | summary |