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510(k) K070560

LRTM SURGICAL MESH by Lifecell Corp. — Product Code FTM

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 11, 2007
Date Received
February 27, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Mesh, Surgical
Device Class
Class II
Regulation Number
878.3300
Review Panel
SU
Submission Type

Other clearances by Lifecell Corp.

  • K130817 — LTN - LAPAROSCOPIC SURGICAL MESH (April 17, 2013)
  • K112534 — LIFECELL TISSUE EXPANDER (August 10, 2012)
  • K121289 — LTM-LABAROSCOPIC SURGICAL MESH (August 3, 2012)
  • K082176 — LTM-BPS SURGICAL MESH (November 14, 2008)
  • K082103 — LTM WOUND DRESSING (October 8, 2008)
  • K080353 — LTM-T SURGICAL MESH (April 3, 2008)
  • K071986 — LTM-RC SURGICAL MESH (October 19, 2007)
  • K061208 — LIFECELL DURAL SUBSTITUTE MATRIX (January 3, 2007)
  • K052735 — ALLOCRAFT DBM (December 28, 2005)

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