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

RESORBABLE CRANIAL CLAMPS

K Number: K021408 · Decision Jul 29, 2002
Classifications
1
FEI Numbers
50
Registration Numbers
50
Same Product Code
28
Applicant Total
402
Review Days
87

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Basic Information

Device Name
RESORBABLE CRANIAL CLAMPS
K Number
K021408
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5250
Medical Specialty
Neurology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes (Usa)
Date Received
May 3, 2002
Decision Date
July 29, 2002
Product Code
GXR
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
GXR Cover, Burr Hole

Similar 510(k) Clearances

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

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Other Clearances by Synthes (Usa)

K Number Device Name
K131984 SYNTHES SYNSONIC ULNA NAIL
K111667 SYNTHES SUPRAPATELLAR INSERTION INSTRUMENTS
K111540 SYNTHES 3.5MM LCP CLAVICLE PLATE SYSTEM
K110789 SYNTHES STERNAL ZIPFIX SYSTEM
K103002 SYNTHES MULTILOC PROXIMAL HUMERAL NAILING SYSTEM
K103243 2.4MM VA-LCP INTERCARPAL FUSION SYSTEM
K102656 SYNTHES DENTOALVEOLAR BONE FIXATION SYSTEM
K093299 SYNTHES ORTHODONTIC BONE ANCHOR SYSTEM
K102694 2.4MM VA-LCP DORSAL DISTAL RADIUS PLATES
K100776 SYNTHES 2.4 MM/2.7 MM VARIABLE ANGLE LCP FOREFOOT/MIDFOOT SYSTEM
Search all 402 clearances from Synthes (Usa) →