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

NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS

K Number: K800494 · Decision Mar 18, 1980
Classifications
1
FEI Numbers
220
Registration Numbers
220
Same Product Code
70
Applicant Total
303
Review Days
14

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Basic Information

Device Name
NEW JERSEY HEMIARTHROPLASTY SHOLDER PROS
K Number
K800494
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3690
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Depuy, Inc.
Date Received
March 4, 1980
Decision Date
March 18, 1980
Product Code
HSD
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
HSD Prosthesis, Shoulder, Hemi-, Humeral, Metallic Uncemented

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Other Clearances by Depuy, Inc.

K Number Device Name
K043058 PINNACLE CONSTRAINED ACETABULAR LINERS
K042664 LPS UPPER EXTREMITY
K041085 LPS (LIMB PRESERVATION SYSTEM) LOWER EXTREMITY DOVETAIL INTERCALARY
K033959 LPS
K040544 DURALOC OPTION ACETABULAR CUP SYSTEM, MODELS 1599-01-044 TO -066, 1599-11-044 TO -062 AND 1599-21-044 TO -062
K021478 DELTA SHOULDER
K033329 DEPUY ACE UNIVERSAL AND TROCH ENTRY FEMORAL NAIL SYSTEMS
K032151 DEPUY SIGMA TIBIAL INSERTS AND CO-CR TIBIAL TRAYS
K020541 AGILITY ANKLE REVISION PROSTHESIS
K011810 ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING
Search all 303 clearances from Depuy, Inc. →