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

BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER

K Number: K040034 · Decision Feb 11, 2004
Classifications
1
FEI Numbers
354
Registration Numbers
354
Same Product Code
302
Applicant Total
45
Review Days
34

Basic Information

Device Name
BLACKSTONE ASCENT POCT SYSTEM LATERAL OFFSET ADAPTER
K Number
K040034
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3070
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BLACKSTONE MEDICAL, INC.
Date Received
January 8, 2004
Decision Date
February 11, 2004
Product Code
MNI
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
MNI Orthosis, Spinal Pedicle Fixation

Similar 510(k) Clearances

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

View all

Other Clearances by BLACKSTONE MEDICAL, INC.

K Number Device Name
K093926 FIREBIRD SPINAL FIXATION SYSTEM
K100614 HALLMARK ANTERIOR CERVCIAL PLATE SYSTEM, HALLMARK FIVE-LEVEL CERVICAL PLATES
K092624 FIREBIRD SPINAL FIXATION SYSTEM
K082797 BLACKSTONE PEDICLE SCREW SYSTEM
K081684 BLACKSTONE PEDICLE SCREW SYSTEM
K082235 BLACKSTONE PILLAR XL PEEK SPACERS
K081849 BLACKSTONE PILLAR SA PARTIAL VERTEBRAL BODY REPLACEMENT DEVICE
K081177 BLACKSTONE MEDICAL, INC., PILLAR SPACER SYSTEM
K080407 BLACKSTONE SFS PARALLEL ROD CONNECTORS
K080394 BLACKSTONE ASCENT POSTERIOR OCCIPITAL CERVICO-THORACIC (POCT) SYSTEM
Search all 45 clearances from BLACKSTONE MEDICAL, INC. →