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

KYPHX HV-R, MODEL C01A

K Number: K033801 · Decision Apr 1, 2004
Classifications
1
FEI Numbers
112
Registration Numbers
112
Same Product Code
106
Applicant Total
9
Review Days
115

Basic Information

Device Name
KYPHX HV-R, MODEL C01A
K Number
K033801
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3027
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
KYPHON, INC.
Date Received
December 8, 2003
Decision Date
April 1, 2004
Product Code
NDN
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
NDN Cement, Bone, Vertebroplasty

Similar 510(k) Clearances

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

View all

Other Clearances by KYPHON, INC.

K Number Device Name
K073516 DISCYPHOR DIRECT CATHETER SYSTEM, DISCYPHOR DIRECT NEEDLES, LONG, DISCYPHOR DIRECT NEEDLES, REGULAR
K063071 DISCYPHOR CATHETER SYSTEM, MODEL D01A; DISCYPHOR INTRODUCER NEEDLE, MODEL D01B
K061210 FUNCTIONAL ANAESTHETIC DISCOGRAPHY (FAD) CATHETER SYSTEM, MODEL D01A ; INTRODUCER NEEDLE, MODEL D01B
K041454 KYPHX XPANDER INFLATABLE BONE TAMPS MODEL#KO8A,KO9A,K13A
K041584 KYPHX HV-R BONE CEMENT, MODEL C01A
K032212 KYPHX DIRECTIONAL INFLATABLE BONE TAMP, MODELS K16A AND K17A
K010246 KYPHX INFLATABLE BONE TAMP, SIZE 20/3,MODEL K01A, KYPHX INFLATABLE BONE TAMP, SIZE 15/3, MODEL K02A
K981251 KYPHON INFLATABLE BONE TAMP