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

FORCEPS

K Number: K771746 · Decision Sep 26, 1977
Classifications
1
FEI Numbers
444
Registration Numbers
445
Same Product Code
103
Applicant Total
303
Review Days
11

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Basic Information

Device Name
FORCEPS
K Number
K771746
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Depuy, Inc.
Date Received
September 15, 1977
Decision Date
September 26, 1977
Product Code
GEN
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
GEN Forceps, General & Plastic Surgery

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K020541 AGILITY ANKLE REVISION PROSTHESIS
K011810 ORTHOGENESIS LPS PROXIMAL TIBIAL REPLACEMENT AND ORTHOGENESIS LPS TIBIAL BEARING
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