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510(k) K023908

INTERPORE CROSS CEMENT RESTRICTOR by Interpore Cross Intl. — Product Code JDK

K023908 is an FDA 510(k) premarket notification submitted by Interpore Cross Intl. for the device "INTERPORE CROSS CEMENT RESTRICTOR". The FDA issued a decision of SESU on May 16, 2003. The device falls under product code JDK (Prosthesis, Hip, Cement Restrictor), a Class II device regulated under 21 CFR 878.3300. Interpore Cross Intl. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESU ()
Decision Date
May 16, 2003
Date Received
November 25, 2002
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Hip, Cement Restrictor
Device Class
Class II
Regulation Number
878.3300
Review Panel
OR
Submission Type

Other clearances by Interpore Cross Intl.

  • K050861 — PEEK CAS (May 27, 2005)
  • K031399 — INTERGRO DBM (February 18, 2005)
  • K041407 — TITANIUM MESH IMPLANT (December 29, 2004)
  • K043229 — MODIFICATION TO ALTIUS OCT SYSTEM (December 21, 2004)
  • K042798 — C-TEK C-TRUN ANTERIOR CERVICAL PLATE SYSTEM (November 4, 2004)
  • K040928 — EXPANDABLE PEEK VBR IMPLANT (August 27, 2004)
  • K041794 — C-TEK C-THRU ANTERIOR CERVICAL PLATE SYSTEM (July 19, 2004)
  • K041449 — SYNERGY HELICAL FLANGE PLUG, HELICAL FLANGE SEAT AND HELICAL FLANGE REDUCTION SE (July 1, 2004)
  • K033961 — ALTIUS OCT SYSTEM (April 14, 2004)
  • K040168 — MODIFICATION TO GEO STRUCTURE (April 8, 2004)

Other clearances for product code JDK

  • K210062 — Mectaplug PE II (April 8, 2021)
  • K061465 — KMI CEMENT RESTRICTOR IMPLANT (October 5, 2006)
  • K061698 — MODIFICATION TO LIFE SPINE CEMENT RESTRICTOR (July 12, 2006)
  • K060247 — LIFE SPINE CEMENT RESTRICTOR (May 11, 2006)
  • K060132 — SPINAL USA CEMENT RESTRICTOR SYSTEM (March 16, 2006)
  • K051371 — INTERBODY INNOVATIONS CEMENT RESTRICTOR (December 6, 2005)
  • K051836 — SKELITE RESORBABLE CEMENT RESTRICTOR (November 21, 2005)
  • K051607 — NOVASPINE CEMENT RESTRICTOR NSCR (October 7, 2005)
  • K052367 — SCIENT'X CEMENT RESTRICTOR (October 5, 2005)
  • K041382 — POLYGRAFT BGS; BONE GRAFT SUBSTITUTE (June 17, 2005)

FDA data resources