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

MODIFIED PODIATRY PRODUCTS

K Number: K771006 · Decision Jun 17, 1977
Classifications
1
FEI Numbers
230
Registration Numbers
230
Same Product Code
20
Applicant Total
9
Review Days
15

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Basic Information

Device Name
MODIFIED PODIATRY PRODUCTS
K Number
K771006
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Dentronix, Inc.
Date Received
June 2, 1977
Decision Date
June 17, 1977
Product Code
HTZ
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
HTZ Instrument, Cutting, Orthopedic

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (HTZ), ordered by most recent decision date.

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Other Clearances by Dentronix, Inc.

K Number Device Name
K910202 DENTRONIX MODEL 2000
K880322 DENTRONIX DDS 5000 DRY HEAT STERILIZATION SYSTEM
K771005 NEW PODIATRY PRODUCTS
K770304 CUTTER, P605 GENERAL PURPOSE
K770302 CUTTER, P606 BONE
K770303 NIPPER, NAIL, P610 ENGLISH
K770305 CUTTER, P607 BONE
K770301 NIPPER, PSO4 TISSUE