FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

COLLAGEN NEUROSPONGE

K Number: K891993 · Decision Mar 23, 1990
Classifications
1
FEI Numbers
33
Registration Numbers
33
Same Product Code
23
Applicant Total
13
Review Days
360

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
COLLAGEN NEUROSPONGE
K Number
K891993
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.4700
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Vitaphore Corp.
Date Received
March 28, 1989
Decision Date
March 23, 1990
Product Code
HBA
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
HBA Neurosurgical Paddie

Similar 510(k) Clearances

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

View all

Other Clearances by Vitaphore Corp.

K Number Device Name
K914579 SILVER FOAM WOUND DRESSING
K913148 COLLAGEN SHIELD FOR ACUTE CARE
K895920 VITAPATCH PIN PROTECTION DEVICE FOR PERCUTANEOUS
K902558 COLLAGEN SHIELD FOR ACUTE CARE
K896455 VITACHOICE WOUND DRESSING
K896046 VITAPATCH CATH. SECUREMENT DEVICE W/CHLORHEXIDINE
K895993 VITAPATCH ANTIMICROBIAL CATHETER SECUREMENT DEVICE
K890435 VITAACCESS CATHETER INTRODUCER KIT
K882100 VITACUFF(R) PERCUTANEOUS INFECT. CONTROL KIT
K872998 VITAACCESS (TM) CATHETER INTRODUCER SYSTEM
Search all 13 clearances from Vitaphore Corp. →