510(k) K771006

Device
MODIFIED PODIATRY PRODUCTS
Applicant
Dentronix, Inc.
510(k) number
K771006
Product code
HTZ
Decision
Substantially Equivalent (SESE)
Decision date
1977-06-17
Date received
1977-06-02
Regulation
878.4800
Classification name
Instrument, Cutting, Orthopedic
Medical specialty
General, Plastic Surgery
Review panel
General, Plastic Surgery
Device class
1
Clearance type
Traditional
Third party reviewed
N

Applicant Contact#

Address
803 N. Front St. Suite 3 Mchenry IL US 60050 60050

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HTZ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K933933CEBOPLANESynvasive Technology, Inc.1994-04-15
K931737HEDLEYL INTRAMEDULLARY PREPARATION BRUSHSynvasive Technology, Inc.1994-01-07
K87088245 DEGREE SHAVERBowen & Company, Inc.1987-03-23
K853678KAMBIN SPINAL INSTRUMENT SETPilling Co.1985-09-24
K850527ARTHROSCOPY SUCTION BIOPSY PUNCHT. Korossurgical Instruments Corp.1985-03-14
K850423CONCEPT SUCTION SLEEVEConcept, Inc.1985-03-14
K841980SIDE CUTTING SERRATED BLADEStainless Mfg., Inc.1984-08-15
K842774CODMAN SUCTION PUNCH-PRODUCT CODESCodman & Shurtleff, Inc.1984-07-27
K841978LATERAL RELEASE KNIFE 5MM & 7MMStainless Mfg., Inc.1984-06-19
K842111KOGAN ENDOSPECULUM 9-1/2J. Sklar Mfg. Co., Inc.1984-06-19
K841982MENISCOTOME 4MM & 5MMStainless Mfg., Inc.1984-06-19
K8419775MM DOUGLE EDGE RING CURETTEStainless Mfg., Inc.1984-06-19
K841976HOOK KNIFE 4MM & 5MMStainless Mfg., Inc.1984-06-19
K841975ROSETTE KNIFE 4MMStainless Mfg., Inc.1984-06-19
K841974RETROGRADE KNIFE 4MM & 5MMStainless Mfg., Inc.1984-06-19