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

CARPENTER BONE CLAMP

K Number: K770118 · Decision Jan 26, 1977
Classifications
1
FEI Numbers
342
Registration Numbers
342
Same Product Code
13
Applicant Total
124
Review Days
5

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Basic Information

Device Name
CARPENTER BONE CLAMP
K Number
K770118
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Stryker Corp.
Date Received
January 21, 1977
Decision Date
January 26, 1977
Product Code
HXD
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
HXD Clamp

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