FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS

K Number: K970567 · Decision Feb 27, 1997
Classifications
1
FEI Numbers
155
Registration Numbers
155
Same Product Code
70
Applicant Total
108
Review Days
14

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
SELECT SHOULDER CURVED-BACK PEGGED ALL POLY GLENOIDS
K Number
K970567
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3650
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Intermedics Orthopedics
Date Received
February 13, 1997
Decision Date
February 27, 1997
Product Code
KWT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KWT), ordered by most recent decision date.

View all

Other Clearances by Intermedics Orthopedics

K Number Device Name
K970300 NATURAL-HIP SYSTEM POROUS STEM WITH HA/CSTI
K970498 NATURAL-KNEE II REVISION FEMORAL SPACER LUGS
K970166 NATURAL-HIP SYSTEM COCR REVISION STEM
K964357 NATURAL-HIP SYSTEM COCR STEM
K964350 MODULA OPTIONS FOR SEVERE BONE LOSS AND TRAUMA
K962190 PATELLOFEMORAL JOINT PROSTHESIS
K963266 NATURAL HIP SYSTEM POROUS STEM - COLLARLESS, COLLARED
K963155 INTERMOORE FRACTURE HIP STEM (MODIFY)
K962315 SELECT SHOULDER COCR HUMERAL STEM COMPONENT
K962289 SELECT SHOULDER COCR HUMERAL STEM COMPONENT
Search all 108 clearances from Intermedics Orthopedics →