The following data is part of a premarket notification filed by Peters Surgical with the FDA for Cardioflon, Cardioxyl.
Device ID | K060163 |
510k Number | K060163 |
Device Name: | CARDIOFLON, CARDIOXYL |
Classification | Suture, Nonabsorbable, Synthetic, Polyethylene |
Applicant | PETERS SURGICAL Z.I. LES VIGNES 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
Contact | Annie Lasserre |
Correspondent | Annie Lasserre PETERS SURGICAL Z.I. LES VIGNES 42 RUE BENOIT FRACHON Bobigny, FR 93013 |
Product Code | GAT |
CFR Regulation Number | 878.5000 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-01-23 |
Decision Date | 2006-10-11 |
Summary: | summary |