Medical Device Manufacturer · US , West Chester , PA

Centinel Spine, Inc. - FDA 510(k) Cleared Devices

10 submissions · 10 cleared · Since 2012

Recent clearances: STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX, ACTILIF C FLX, ACTILIF M FLX, ACTILIF L FLX and ACTILIF Lateral-Oblique FLX

Total

Cleared

Denied

Centinel Spine, Inc. has 10 FDA 510(k) cleared orthopedic devices. Based in West Chester, US.

Historical record: 10 cleared submissions from 2012 to 2018.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

510(k) submissions have been managed by Musculoskeletal Clinical Regulatory Advisers, LLC as regulatory consultant.

Centinel Spine, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.

FDA 510(k) Regulatory Record - Centinel Spine, Inc.

10 devices

1-10 of 10

Cleared May 08, 2018

STALIF C FLX, STALIF M FLX, STALIF L FLX and STALIF Lateral-Oblique FLX,...

Centinel Spine STALIF TT, STALIF MIDLINE, MIDLINE II, MIDLINE II-Ti

Centinel Spine, Inc. - FDA 510(k) Cleared Devices

FDA 510(k) Regulatory Record - Centinel Spine, Inc.

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