ClearanceBrief
Company ยท US

Sutter Corp.

FDA 510(k) clearances and medical device recalls filed under this name, 1989 to 1995. Name variants (Inc, Corp, punctuation) are merged.

7510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
BXBExerciser, Powered5
KWHProsthesis, Toe, Constrained, Polymer1
KYJProsthesis, Finger, Constrained, Polymer1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Jun 12, 1995K943354SUTTER HAMMERTOE JOINT PROSTHESIS
Sutter Corp.
KWH
Feb 27, 1995K945221SUTTER MODEL 6000 HAND CPM DEVICE
Sutter Corp.
BXB
Mar 10, 1994K931588SUTTER PROXIMAL INTERPHALANGEAL JOINT
Sutter Corp.
KYJ
Feb 22, 1993K924654FIRST METATARSOPHALANGEAL JOINT MOTION SPLINT
Sutter Corp.
BXB
Jan 8, 1992K914860SUTTER MODEL 10000 LEG CPM DEVICE
Sutter Corp.
BXB
Jul 25, 1990K902707MODEL 9000 AT ANKLE CPM DEVICE
Sutter Corp.
BXB
Feb 27, 1989K890607SUTTER HOSPITAL CPM
Sutter Corp.
BXB

Latest recalls

DateFirm and productCodeLinked 510(k)
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