FDA 510(k)
FDA class 2
Substantially Equivalent for Some Indications
🇬🇧 United Kingdom
PRODEK
K Number: K953609
·
Decision Jan 31, 1996
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
84
Applicant Total
11
Review Days
182
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Basic Information
- Device Name
- PRODEK
- K Number
- K953609
- Device Class
- FDA class 2
- Clearance Type
- Traditional
- Regulation Number
- 878.5010
- Medical Specialty
- General, Plastic Surgery
- Decision
- Substantially Equivalent for Some Indications
- Applicant
- Sutures , Ltd.
- Date Received
- August 2, 1995
- Decision Date
- January 31, 1996
- Product Code
- GAW
- Advisory Committee
- General, Plastic Surgery
- Review Advisory Committee
- SU
- Third Party
- N
Classifications
This FDA 510(k) entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| GAW | Suture, Nonabsorbable, Synthetic, Polypropylene | FDA class 2 | General, Plastic Surgery |
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Other Clearances by Sutures , Ltd.
| K Number | Device Name | ||
|---|---|---|---|
| K990432 | SURGISORB | May 27, 1999 | Substantially Equivalent for Some Indications |
| K943216 | SURGIDEK | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943222 | SURGIDEK S | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943218 | CHROMIC CATGUT | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943223 | SURGIDEK B | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943221 | SURGIBOND | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943217 | PLAIN CATGUT | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943627 | SURGISILK | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K943220 | SUTULENE | Dec 5, 1994 | Substantially Equivalent for Some Indications |
| K865038 | SURGISTEEL | Jun 30, 1987 | Substantially Equivalent |