FDA 510(k) FDA class 2 Substantially Equivalent 🇬🇧 United Kingdom

DOUBLEPLAY SUTURE ANCHOR

K Number: K061949 · Decision Sep 25, 2006
Classifications
1
FEI Numbers
653
Registration Numbers
653
Same Product Code
1040
Applicant Total
23
Review Days
77

Basic Information

Device Name
DOUBLEPLAY SUTURE ANCHOR
K Number
K061949
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOCOMPOSITES LTD.
Date Received
July 10, 2006
Decision Date
September 25, 2006
Product Code
HWC
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

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Other Clearances by BIOCOMPOSITES LTD.

K Number Device Name
K141830 STIMULAN KIT, STIMULAN RAPID CURE
K082381 GENEX
K082383 FORTOSS VITAL
K073341 GENEX PUTTY
K081428 MODIFICATION TO DOUBLEPLAY SUTURE ANCHOR
K072127 DOMINATOR
K071952 GRAFTLOCK SCREW, ST SCREW
K071091 MODIFICATION TO BILOK SCREW
K071115 MODIFICATION TO BILOK ST SCREW
K061311 ALLOGRAN-R
Search all 23 clearances from BIOCOMPOSITES LTD. →