IMPLANET: CE Mark and FDA Clearance in the United States for New JAZZ Diameters

Extension of the JAZZ Band™ technological platform: from a single 5.5 mm diameter implant to the market’s most comprehensive range of sublaminar implants

BORDEAUX, France & BOSTON--()--Regulatory News:

IMPLANET (Paris:IMPL) (Euronext: IMPL, FR0010458729, PEA-PME eligible), a medical technology company specializing in vertebral and knee-surgery implants, today announces that it has obtained regulatory clearance from the FDA (Food and Drug Administration) to market its 3.5 mm, 4.0 mm, 4.5 mm and 6 mm JAZZ rods in the United States and the CE mark in Europe, adding to the original 5.5 mm diameter clearance.

A significant milestone in Implanet’s development strategy, this clearance addresses the treatment of adolescent scoliosis, the first clinical indication targeted by the Company, but also the treatment of deformity and degenerative spinal disorders in adults. Combined with the CE mark obtained in late April 2015, these clearances allow JAZZ to now be a true technological platform – JAZZ Band® – comprising the most comprehensive range of sublaminar implants on the market, providing surgeons rod diameter flexibility depending on the disorder being treated.

Ludovic Lastennet, CEO of Implanet, says: “The implantation of more than 6,000 JAZZ devices in a single 5.5 mm diameter version since its launch in late 2013 is an impressive achievement for the Company. Reaching this latest regulatory milestone will enable us to better serve our customers with a comprehensive product range and to accelerate our deployment, not only in the United States but across all global markets. Our proprietary single-screw design provides optimal tensioning of the band, ensuring robust fixation, controlled by a simple and highly-efficient tensioning instrument. Multiple papers published in 2015 substantiate JAZZ’s clinical efficacy in the treatment of scoliosis, while an independent medico-economic study published in March confirmed the economic benefit of hybrid constructs consisting of screws and sublaminar implants. This economic advantage, combined with a comprehensive range of JAZZ implants, will enable us to achieve our objectives in a global environment where healthcare expenses are subject to more and more stringent controls.

Next financial press release: revenue for the 1st half of 2015, on July 28, 2015

About IMPLANET
Founded in 2007, IMPLANET is a medical technology company that manufactures high-quality implants for orthopedic surgery. Its flagship product, the JAZZ latest-generation implant, aims to treat spinal pathologies requiring vertebral fusion surge Protected by four families of international patents, JAZZ has obtained 510(k) regulatory clearance from the Food and Drug Administration (FDA) in the United States and the CE mark. IMPLANET employs 45 staff and recorded 2014 sales of €7.0 million. For further information, please visit www.implanet.com.

Based near Bordeaux in France, IMPLANET established a US subsidiary in Boston in 2013.

IMPLANET is listed on Compartment C of the Euronext™ regulated market in Paris.
Ticker: IMPL - ISIN code: FR0010458729

Contacts

IMPLANET
Ludovic Lastennet
CEO
Tel.: +33 (0)5 57 99 55 55
investors@implanet.com
or
NewCap
Investor Relations
Florent Alba
Tel.: +33 (0)1 44 71 94 94
implanet@newcap.fr
or
NewCap
Press Relations
Nicolas Merigeau
Tel.: +33 (0)1 44 71 94 98
implanet@newcap.fr

Contacts

IMPLANET
Ludovic Lastennet
CEO
Tel.: +33 (0)5 57 99 55 55
investors@implanet.com
or
NewCap
Investor Relations
Florent Alba
Tel.: +33 (0)1 44 71 94 94
implanet@newcap.fr
or
NewCap
Press Relations
Nicolas Merigeau
Tel.: +33 (0)1 44 71 94 98
implanet@newcap.fr