510(k) K242187

Device
BioBrace®
Applicant
Conmed Corporation
510(k) number
K242187
Product code
OWW
Decision
Substantially Equivalent (SESE)
Decision date
2024-11-27
Date received
2024-07-25
Regulation
878.3300
Classification name
Mesh, Surgical, Absorbable, Orthopaedics, Reinforcement Of Tendon
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
Dionne Sanders
Address
525 French Rd. Utica NY US 13502 13502

FDA Registration Numbers

Source Documents

510(k) summary PDF

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