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

THERMO-PLASTIC SHAVER BLADES

K Number: K963332 · Decision Oct 11, 1996
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
92
Review Days
49

Basic Information

Device Name
THERMO-PLASTIC SHAVER BLADES
K Number
K963332
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Endoscopy
Date Received
August 23, 1996
Decision Date
October 11, 1996
Product Code
HRX
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
HRX Arthroscope

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