FDA 510(k) FDA class 3 Substantially Equivalent 🇺🇸 United States

KIRSCHNER SELF-TAPPING ACETABULAR CUP

K Number: K852351 · Decision Aug 9, 1985
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
113
Applicant Total
76
Review Days
70

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Basic Information

Device Name
KIRSCHNER SELF-TAPPING ACETABULAR CUP
K Number
K852351
Device Class
FDA class 3
Clearance Type
Traditional
Regulation Number
888.3330
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Kirschner Medical Corp.
Date Received
May 31, 1985
Decision Date
August 9, 1985
Product Code
KWA
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
KWA Prosthesis, Hip, Semi-Constrained (Metal Uncemented Acetabular Component)

Similar 510(k) Clearances

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

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Other Clearances by Kirschner Medical Corp.

K Number Device Name
K940537 KIRSCHNER(R) MODULAR II-C(TM) TOTAL SHOULDER SYSTEM
K936274 KIRSCHNER PERFORMANCE POSTERIOR STABILIZED TOTAL KNEE SYSTEM
K942891 SUMMIT TOTAL HIP SYSTEM
K941486 INTEGRITY TOTAL HIP SYSTEM, NON-POROUS
K933843 LINE EXTENSION FOR KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM, POROUS COATED
K935951 KIRSCHNER C-2 OSTEOCAP TOTAL HIP SYSTEM
K935206 KIRSCHNER INTEGRITY ACETABULAR CUP MODIFICATION
K934589 KIRSCHNER PERFORMANCE TOTAL KNEE SYSTEM POROUS COATED
K934694 KIRSCHNER ZIRCONIA FEMORAL HEAD
K920188 THREADED PINS
Search all 76 clearances from Kirschner Medical Corp. →