Skip to content

Company · US

Sutter Biomedical, Inc.

FDA 510(k) clearances and medical device recalls filed under this name, 1981 to 1988. Name variants (Inc, Corp, punctuation) are merged.

11510(k) clearances (0 in 12 months)

0recalls (0 in 12 months)

0recalls that name a 510(k)

Product codes

Code	Device	Records
BXB	Exerciser, Powered	4
KWD	Prosthesis, Toe, Hemi-, Phalangeal	2
JDI	Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented	1
JFA	Exerciser, Finger, Powered	1
KWH	Prosthesis, Toe, Constrained, Polymer	1
KYJ	Prosthesis, Finger, Constrained, Polymer	1
MDM	Instrument, Manual, Surgical, General Use	1

Latest 510(k) clearances

Decided	510(k)	Device and applicant	Code
Feb 3, 1988	K875249	SUTTER PHALANGEAL CAP Sutter Biomedical, Inc.	KWD
Oct 9, 1987	K870200	SUTTER FINGER JOINT PROSTHESIS Sutter Biomedical, Inc.	KYJ
Sep 8, 1986	K861983	SUTTER LESSER METATARSAL CAP Sutter Biomedical, Inc.	KWD
Apr 25, 1985	K850274	SUTTER CPM 9000 -NONMEASURING EXERCISE EQUIPMENT Sutter Biomedical, Inc.	BXB
Apr 12, 1983	K830974	SUTTER CPM 5000 Sutter Biomedical, Inc.	JFA
Mar 17, 1983	K830649	SUTTER CPM 2000 Sutter Biomedical, Inc.	BXB
Jan 14, 1983	K823539	SUTTER CPM Sutter Biomedical, Inc.	BXB
May 21, 1982	K820813	LESSER METATARSAL PHALANG. JOINT PROSTH Sutter Biomedical, Inc.	KWH
Jan 28, 1982	K820083	SUTTER CPM Sutter Biomedical, Inc.	BXB
Nov 16, 1981	K812691	SILICONE IMPLANTS Sutter Biomedical, Inc.	MDM
Oct 14, 1981	K802342	PROXIMAL INTERPHALANGEAL JOINT IMPLANT Sutter Biomedical, Inc.	JDI

Latest recalls

Date	Firm and product	Code	Linked 510(k)
No recalls in this window.

Get alerts for these product codes