Last synced on 18 April 2025 at 11:05 pm

Prosthesis, Tendon, Passive

Page Type
Product Code
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3025
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

CFR § 888.3025 Passive tendon prosthesis

§ 888.3025 Passive tendon prosthesis.

(a) Identification. A passive tendon prosthesis is a device intended to be implanted made of silicon elastomer or a polyester reinforced medical grade silicone elastomer intended for use in the surgical reconstruction of a flexor tendon of the hand. The device is implanted for a period of 2 to 6 months to aid growth of a new tendon sheath. The device is not intended as a permanent implant nor to function as a replacement for the ligament or tendon nor to function as a scaffold for soft tissue ingrowth.

(b) Classification. Class II.

Prosthesis, Tendon, Passive

Page Type
Product Code
Regulation Medical Specialty
Orthopedic
Review Panel
Orthopedic
Submission Type
510(K)
Device Classification
Class 2
Regulation Number
888.3025
GMP Exempt?
No
Summary Malfunction Reporting
Eligible
Implanted Device
Yes
Life-Sustain/Support Device
No
Third Party Review
Not Third Party Eligible

CFR § 888.3025 Passive tendon prosthesis

§ 888.3025 Passive tendon prosthesis.

(a) Identification. A passive tendon prosthesis is a device intended to be implanted made of silicon elastomer or a polyester reinforced medical grade silicone elastomer intended for use in the surgical reconstruction of a flexor tendon of the hand. The device is implanted for a period of 2 to 6 months to aid growth of a new tendon sheath. The device is not intended as a permanent implant nor to function as a replacement for the ligament or tendon nor to function as a scaffold for soft tissue ingrowth.

(b) Classification. Class II.