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510(k) K791960

Device
Roth-kennedy Passer
Applicant
3M COMPANY
510(k) number
K791960
Product code
HWQ
Decision
Substantially Equivalent (SESE)
Decision date
1979-10-04
Date received
1979-10-01
Regulation
888.4540
Classification name
Passer
Medical specialty
Orthopedic
Review panel
Orthopedic
Device class
1
Clearance type
Traditional
Third party reviewed
No

Applicant Contact#

Address
8124 Pacific Ave. White City OR US 97503 97503

FDA Registration Numbers#

Source Documents#

510(k) summary PDF not indicated by FDA

Other 510(k) Records For Product Code HWQ#

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K970360MITEK SUTURE RETROGRADERMitek Products1997-03-10
K920621ACUFEX PASSING PINS AND SURGICAL WIREAcufex Microsurgical, Inc.1993-05-05
K923381SOFT TISSUE EXPANDERAcufex Microsurgical, Inc.1993-05-05
K885311MENISCUS MENDER II LOOPInstrument Makar, Inc.1989-02-09
K843592VICO MICRO SURGICAL INSTRUMENTSVisitec Co.1984-10-05
K841622SOFT-TISSUE INSTRUMENTPlastafil, Inc.1984-07-11
K841623SLOTTED SOFT-TISSUE INSTRUMENTPlastafil, Inc.1984-07-11
K811679SILASTIC TENDON PASSER H.P.Dow Corning Corp. Healthcare Industries Materials1981-07-10