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510(k) K050767

STERLING INTERFERENCE SCREW ST by Regeneration Technologies, Inc. — Product Code HWC

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 9, 2005
Date Received
March 25, 2005
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Screw, Fixation, Bone
Device Class
Class II
Regulation Number
888.3040
Review Panel
OR
Submission Type

Other clearances by Regeneration Technologies, Inc.

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  • K072238 — BIOSET XCH (January 25, 2008)
  • K072327 — CANCELLO-PURE BONE WEDGE, 12MM EVANS OR 6MM COTTON (October 24, 2007)
  • K063584 — STERLING IF SCREW EYELET, MODEL CID3936 AND STERLING CROSS-PIN EYELET, MODEL CID (May 9, 2007)
  • K060180 — BIOSET XC (September 6, 2006)
  • K060253 — STERLING INTERFERENCE SCREW HT, STERLING INTERFERENCE SCREW ST. (February 23, 2006)
  • K052405 — STERLING INTERFERENC SCREW HT (November 16, 2005)
  • K051615 — STERLING CANCELLOUS CHIPS; STERLING CANCELLOUS CUBES (August 15, 2005)
  • K043421 — OPTEFORM, OSTEOFIL, RTI ALLOGRAFT PASTE IC, RTI ALLOGRAFT STRIP IC (February 16, 2005)
  • K043420 — OSTEOFIL, OPTEFIL, REGENAFIL, RTI ALLOGRAFT PASTE (February 10, 2005)

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