The following data is part of a premarket notification filed by Peters Surgical with the FDA for Corolene.
Device ID | K052701 |
510k Number | K052701 |
Device Name: | COROLENE |
Classification | Suture, Nonabsorbable, Synthetic, Polypropylene |
Applicant | PETERS SURGICAL 42 RUE BENOIT FRANCHON Bobigny, FR 93013 |
Contact | Annie Lasserre |
Correspondent | Annie Lasserre PETERS SURGICAL 42 RUE BENOIT FRANCHON Bobigny, FR 93013 |
Product Code | GAW |
CFR Regulation Number | 878.5010 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2005-09-28 |
Decision Date | 2005-12-13 |
Summary: | summary |