ClearanceBrief
Company ยท DE

Heinz Kurz

FDA 510(k) clearances and medical device recalls filed under this name, 1997 to 2001. Name variants (Inc, Corp, punctuation) are merged.

5510(k) clearances (0 in 12 months)
0recalls (0 in 12 months)
0recalls that name a 510(k)

Product codes

CodeDeviceRecords
ETBProsthesis, Partial Ossicular Replacement4
KHJPolymer, Ent Synthetic-Polyamide (Mesh Or Foil Material)1

Latest 510(k) clearances

Decided510(k)Device and applicantCode
Mar 8, 2001K010442KURZ ANGULAR PISTON-TITANIUM PROSTHESIS, MODELS 1006 600, 1006 601, 1006 602, 1006 650, 1006 651, 1006 652
Heinz Kurz, NL
ETB
May 18, 1999K991324TITANIUM VOCAL FOLD MEDIALIZING IMPLANT, MODELS 5001 001 (FEMALE), AND 5001 003 (MALE)
Heinz Kurz, DE
KHJ
Mar 31, 1999K990923TUBINGEN TITANIUM PROSTHESIS (TTP) VARIO, MODELS AERIAL 1004 010 & BELL 1002 010
Heinz Kurz, DE
ETB
Nov 21, 1997K973356K-PISTON WITH BAND HOOK /ANGULAR PISTON
Heinz Kurz, DE
ETB
Aug 4, 1997K972492BELL PROSTHESIS (PARTIAL)
Heinz Kurz, DE
ETB

Latest recalls

DateFirm and productCodeLinked 510(k)
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