ULTIMATE COMPRESSION SCREW SYSTEM

FDA 510(k) Premarket Notification · Submission K972722 · Applicant: Orthopedic Designs, Inc.

Public Record 510(k) Submission Decision Date: 1998-01-23 510(k) record compiled from public FDA source records.

Submission Details & Decision

Normalized public record details for 510(k) notification K972722.

Source Dataset
FDA 510(k) Premarket Notifications
510(k) Number
K972722
Applicant / Sponsor
Device Name
ULTIMATE COMPRESSION SCREW SYSTEM
Product Code
HWC
Decision Date
1998-01-23
Decision / Status
Substantially Equivalent for Some Indications (SN)
Advisory Committee
Orthopedic (OR)
Clearance Type
Traditional
Third Party Flag
N
Date Received
1997-07-21

Related Establishments / Registrations

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