SEARCH RESULTS FOR: (*EPS Shape Moulding Machine*)(7624 results)

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Company Name Brand Name GMDN Term Name GMDN Term Status FDA Product Code Name FDA Product Code Device Packaged As Sterile Sterilization Prior To Use Issuing Agency Device Size Device Size Type Device Class Implantable

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PRINCETON - 00810158212497

RASP/OSTEOTOME ADSON FLAT STRAIGHT 6.75"
Princeton Medical Group, Inc.
33754-17
In Commercial Distribution

  • 00810158212497 ()


  • Orthopaedic osteotome

PRINCETON - 00810158212251

ELEVATOR BOIES PERIOSTEAL 9MM 7.5
Princeton Medical Group, Inc.
33720-19
In Commercial Distribution

  • 00810158212251 ()


  • Orthopaedic osteotome

PRINCETON - 00810158212022

OSTEOTOME LAMBOTTE 13MM CURVED 9"
Princeton Medical Group, Inc.
33651-13
In Commercial Distribution

  • 00810158212022 ()


  • Orthopaedic osteotome

PRINCETON - 00810158212008

ELEVATOR MCGLAMRY 11MM 6.5"
Princeton Medical Group, Inc.
33762-11
In Commercial Distribution

  • 00810158212008 ()


  • Orthopaedic osteotome

Expanding Innovations - 00810166520119

Osteotome, Straight
EXPANDING INNOVATIONS, INC.
EI3859
In Commercial Distribution

  • 00810166520119 ()


  • Orthopaedic osteotome

Pisces-SA - B06217607038

Osteotome
Osseus Fusion Systems, LLC
1760-7038
In Commercial Distribution

  • B06217607038 ()
1760-7038

  • Orthopaedic osteotome

EARP INSTRUMENTS - 00810135960649

RETRACTABLE OSTEOTOME. The EARP Interbody System is intended for intervertebral body fusion in the lumbar spine in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels from L2 to S1 of the lumbosacral spine. DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. These patients should have had six months of non-operative treatment prior to treatment with an intervertebral cage. DDD patients may also have Grade 1 spondylolisthesis or retrolisthesis at involved levels. The device system must be used with supplemental fixation and autograft to facilitate fusion and is implanted via a posterolateral approach.
NVISION BIOMEDICAL TECHNOLOGIES, INC.
EARP-O
In Commercial Distribution

  • 00810135960649 ()


  • Orthopaedic osteotome

INSTRUMENT - 07613327310917

SPECIALTY TRIATHLON POSTERIOR OSTEOTOME
Howmedica Osteonics Corp.
I-K2030KF02
In Commercial Distribution

  • 07613327310917 ()

  • Width: 25.0 Millimeter
I-K2030KF02

  • Orthopaedic osteotome

INSTRUMENT - 07613327310825

SPECIALTY TRIATHLON POSTERIOR OSTEOTOME
Howmedica Osteonics Corp.
I-K2030KF01
In Commercial Distribution

  • 07613327310825 ()

  • Width: 22.0 Millimeter
I-K2030KF01

  • Orthopaedic osteotome

INSTRUMENT - 07613327249590

MODULAR BOX OSTEOTOME
Howmedica Osteonics Corp.
1601-1210
In Commercial Distribution

  • 07613327249590 ()
1601-1210

  • Orthopaedic osteotome
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