FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

OSTEONICS INSIGHT KNEE POSITIONING & ALIGNMENT SYSTEM

K Number: K953961 · Decision Nov 29, 1995
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
5
Applicant Total
178
Review Days
99

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Basic Information

Device Name
OSTEONICS INSIGHT KNEE POSITIONING & ALIGNMENT SYSTEM
K Number
K953961
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4960
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Osteonics Corp.
Date Received
August 22, 1995
Decision Date
November 29, 1995
Product Code
FWW
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FWW Table, Operating-Room, Pneumatic

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