Medtronic’s (MDT) Prestige LP cervical disc received FDA Premarket Approval for 2-level cervical disc replacement.
Seven-year follow-up data, announced in 2Q16, demonstrated favorable clinical outcomes and patient satisfaction for Prestige LP vs. 2-level anterior cervical discectomy and fusion (ACDF).
The device, which received approval for 1-level cervical disc replacement in 2014, is the third cervical disc in MDT’s portfolio, alongside BRYAN and Prestige ST.
Prestige LP and LDR’s Mobi-C are the only two cervical discs approved for 2-level cervical disc replacement in the U.S. In late 2Q16, Zimmer Biomet announced its intent to acquire LDR.
Medtronic's (MDT) Prestige LP cervical disc received FDA Premarket Approval for 2-level cervical disc replacement.
Seven-year follow-up data, announced in 2Q16, demonstrated favorable clinical outcomes and patient satisfaction for Prestige LP vs. 2-level anterior cervical discectomy and fusion (ACDF).
The device, which received approval for...
Medtronic’s (MDT) Prestige LP cervical disc received FDA Premarket Approval for 2-level cervical disc replacement.
Seven-year follow-up data, announced in 2Q16, demonstrated favorable clinical outcomes and patient satisfaction for Prestige LP vs. 2-level anterior cervical discectomy and fusion (ACDF).
The device, which received approval for 1-level cervical disc replacement in 2014, is the third cervical disc in MDT’s portfolio, alongside BRYAN and Prestige ST.
Prestige LP and LDR’s Mobi-C are the only two cervical discs approved for 2-level cervical disc replacement in the U.S. In late 2Q16, Zimmer Biomet announced its intent to acquire LDR.
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