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 |