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

HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS

K Number: K871685 · Decision Jun 12, 1987
Classifications
1
FEI Numbers
68
Registration Numbers
69
Same Product Code
257
Applicant Total
31
Review Days
44

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Basic Information

Device Name
HEYER-SCHULTE SPETZLER LUMBAR-PERITONEAL SHUNT SYS
K Number
K871685
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.5550
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
American V. Mueller
Date Received
April 29, 1987
Decision Date
June 12, 1987
Product Code
JXG
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
JXG Shunt, Central Nervous System And Components

Similar 510(k) Clearances

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

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Other Clearances by American V. Mueller

K Number Device Name
K873771 HEYER-SCHULTE(R) ONE PIECE SHUNT VENT. CATH. INTRO
K873332 MAXIVAC(TM) CLOSED WOUND SUCTION DRAINAGE SYSTEM
K864676 HEYER-SCHULTE HERMETIC EXTERNAL CSF DRAIN. SYSTEM
K862772 V. MUELLER (R) GOOSENECK CIRCULAR STAPLER
K861471 V. MUELLER VITAL CLIP-HEMOSTATIC CLIP
K854568 V. MUELLER PNEUMO-INTESTINAL 15 VASCULAR & 30 STAP
K854049 HEYER-SCHULTE SYRINGO PERITONEAL SHUNT
K851082 V. MUELLER BLOM-SINGER ESOPHAGEAL INSUFFLATION TES
K851974 V. MUELLER VITAL SKIN STAPLER
K850947 V-MUELLER INVERTED LINEAR ANASTOMOSIS INSTRUMENTS
Search all 31 clearances from American V. Mueller →