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In Situ Polymerizing Peripheral Nerve Repair Device

Page Type
Product Code
Definition
An in situ polymerizing peripheral nerve repair device is intended for the sutureless repair of peripheral nerve injuries.
Physical State
The device consists of a polymeric, sterile, absorbable, component which is polymerized in situ using an externally applied process, energy source, or chemical.
Technical Method
The device is prepared, placed at the target nerve repair location, and polymerized in situ at the time of the surgery. Polymerization is initiated using an externally applied process, energy source, or chemical to form a crosslinked polymer at and/or around the injured peripheral nerve.
Target Area
Peripheral Nerves
Regulation Medical Specialty
Neurology
Review Panel
Neurology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
882.5270
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 SFD is linked to regulation 21CFR882.5270, which does not seem to exist yet. It may be pending at the moment.

In Situ Polymerizing Peripheral Nerve Repair Device

Page Type
Product Code
Definition
An in situ polymerizing peripheral nerve repair device is intended for the sutureless repair of peripheral nerve injuries.
Physical State
The device consists of a polymeric, sterile, absorbable, component which is polymerized in situ using an externally applied process, energy source, or chemical.
Technical Method
The device is prepared, placed at the target nerve repair location, and polymerized in situ at the time of the surgery. Polymerization is initiated using an externally applied process, energy source, or chemical to form a crosslinked polymer at and/or around the injured peripheral nerve.
Target Area
Peripheral Nerves
Regulation Medical Specialty
Neurology
Review Panel
Neurology
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
882.5270
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 SFD is linked to regulation 21CFR882.5270, which does not seem to exist yet. It may be pending at the moment.