Y-Knot OneStep Anchor

FDA 510(k) Premarket Notification · Submission K193606 · Applicant: Conmed Corporation

Public Record 510(k) Submission Decision Date: 2020-01-22 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K193606.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K193606
Applicant / Sponsor
Device Name
Y-Knot OneStep Anchor
Product Code
MBI
Decision Date
2020-01-22
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Orthopedic (OR)
Clearance Type
Special
Third Party Flag
N
Date Received
2019-12-23

Related Establishments / Registrations

Public Record Disclaimer

This page represents an index of public-record FDA premarket notification filings. AvaSpecs is a private aggregator and is not affiliated with the FDA or any government agency. This page does not constitute medical, safety, legal, regulatory, or compliance advice. Information may be outdated or incomplete. Refer to official government source files for critical decisions.

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