PROVEN MODULAR TIBIAL TRAY

FDA 510(k) Premarket Notification · Submission K030577 · Applicant: Stelkast Company

Public Record 510(k) Submission Decision Date: 2003-03-25 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K030577.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K030577
Applicant / Sponsor
Device Name
PROVEN MODULAR TIBIAL TRAY
Product Code
JWH
Decision Date
2003-03-25
Decision / Status
Substantially Equivalent (SESE)
Advisory Committee
Orthopedic (OR)
Clearance Type
Special
Third Party Flag
N
Date Received
2003-02-24

Related Establishments / Registrations

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