Last synced on 12 October 2025 at 8:21 pm

Absorbable Gel For Intraoperative Use In Spine Surgery

Page Type
Product Code
Definition
This device is an absorbable gel implant for intraoperative use in spinal procedures that is applied to nerve roots after hemostasis has been achieved and prior to closure. The device is intended as an adjunct to the surgical procedure to reduce pain and neurological symptoms.
Physical State
The device is an absorbable, clear, flowable, viscoelastic gel.
Technical Method
The device is applied during lumbar spine surgery to coat and protect the sensory nerves and isolate them from the surrounding tissues and fluid, providing post-surgical reduction in surface exposure of the nerves to irritants and proinflammatory mediators that may cause pain
Target Area
Spine
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3047
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QVL is linked to regulation 21CFR888.3047, which does not seem to exist yet. It may be pending at the moment.

Absorbable Gel For Intraoperative Use In Spine Surgery

Page Type
Product Code
Definition
This device is an absorbable gel implant for intraoperative use in spinal procedures that is applied to nerve roots after hemostasis has been achieved and prior to closure. The device is intended as an adjunct to the surgical procedure to reduce pain and neurological symptoms.
Physical State
The device is an absorbable, clear, flowable, viscoelastic gel.
Technical Method
The device is applied during lumbar spine surgery to coat and protect the sensory nerves and isolate them from the surrounding tissues and fluid, providing post-surgical reduction in surface exposure of the nerves to irritants and proinflammatory mediators that may cause pain
Target Area
Spine
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3047
GMP Exempt?
No
Summary Malfunction Reporting
Ineligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

No Linked CFR Text

Product code QVL is linked to regulation 21CFR888.3047, which does not seem to exist yet. It may be pending at the moment.