510(k) K233355

Device
Cypris eXact Suturing System
Applicant
Cypris Medical
510(k) number
K233355
Product code
GAW
Decision
Substantially Equivalent (SESE)
Decision date
2024-01-12
Date received
2023-09-29
Regulation
878.5010
Classification name
Suture, Nonabsorbable, Synthetic, Polypropylene
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Related Records

Applicant Contact

Contact
Dan Holton
Address
4541 N. Ravenswood Ave., #202 Chicago IL US 60640 60640

FDA Registration Numbers

Source Documents

510(k) summary PDF

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