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

PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER

K Number: K961853 · Decision Jun 21, 1996
Classifications
1
FEI Numbers
368
Registration Numbers
368
Same Product Code
669
Applicant Total
78
Review Days
38

Basic Information

Device Name
PROLINE FAST PASS ARTHOSCOPIC NEEDLE PASSER
K Number
K961853
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.1100
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
ACUFEX MICROSURGICAL, INC.
Date Received
May 14, 1996
Decision Date
June 21, 1996
Product Code
HRX
Advisory Committee
Orthopedic
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
HRX Arthroscope

Similar 510(k) Clearances

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

View all

Other Clearances by ACUFEX MICROSURGICAL, INC.

K Number Device Name
K961555 ACUFEX TAG BIOABSORBABLE ANCHORS
K954246 ACUFEX ENDOFIX ABSORBABLE INTERFERENCE SCREW
K952535 ACUFEX ENDOBUTTON TAPE
K953276 ACUFEX TAG DELIVERY SYSTEM
K953459 ACUFEX TAG ANCHOR
K941740 ACUFEX ROTATOR CUFF FIXATION BUTTON
K944500 ACUFEX PATELLAR BONE BLOCK SIZER
K951859 ACUFEX ENDOBUTTON PACK
K946346 ACUFEX TAG(R) BIOABSORBABLE ANCHORS
K941709 ACUFEX ARTHROSCOPIC DISCECTOMY SYSTEMS
Search all 78 clearances from ACUFEX MICROSURGICAL, INC. →